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Warning issued as Xanax recalled nationwide, FDA announces The FDA has designated it a class II recall.

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⚠️ Class II Recall: FAILED DISSOLUTION SPECIFICATIONS

Viatris Specialty LLC
*XANAX XR 3 mg - 60 ct bottles

Dist to wholesalers + retailers (pharmacies): NATIONWIDE

4-16-26
www.newsweek.com/warning-issu...

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Vitaquest Iron Supplements Recalled For Poisoning Risk Vitaquest iron supplements are being recalled for poisoning risk. The packaging is not child-resistant, which poses a risk of serious injury or death from

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⚠️ Recall: CHILD POISONING RISK
Packaging is NOT child-resistant

Vitaquest International
IRON-CONTAINING SUPPLEMENTS
*11 Brands

Dist: NATIONWIDE

4-15-26
foodpoisoningbulletin.com/2026/vitaque...

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FDA Issues Nationwide Recall for Popular Cough Drops - Here's the Full List And what to do if you find them in your medicine cabinet.

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⚠️ Class II Recall: PRODUCTS DO NOT MEET FDA STANDARDS

Xiamen Kang Zhongshan Biotechnology Co. Ltd
*COUGH DROPS - sold under 5 BRAND NAMES

4-15-26
www.goodhousekeeping.com/health/a7101...

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A product photo of the packaging for Morovan brand Gel Nail Polish Remover, which is implicated in a recall for containing the prohibited hazardous substances of Methylene Chloride and Chloroform.

Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including company contact information.

A product photo of the packaging for Morovan brand Gel Nail Polish Remover, which is implicated in a recall for containing the prohibited hazardous substances of Methylene Chloride and Chloroform. Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including company contact information.

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⚠️ Recall: Prohibited Hazardous Substances
METHYLENE CHLORIDE + CHLOROFORM

HongKong Yiixin Trading Ltd
*MOROVAN brand GEL NAIL POLISH REMOVER

Sold on AMAZON.COM
8-2025 thru 1-2026

4-13-26
www.fda.gov/safety/recal...

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*Some Boxed Hair Dyes Contain Fewer Toxins Than Others
~ Consumer Reports

🦋 Follow: @consumerreports.org

4-14-26

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Fluoride in drinking water has no effect on IQ or brain function, long-term study shows The new research is the first to measure community water fluoridation exposure during childhood and any potential impact on cognition up to age 80.

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*Flouride in drinking water has no effect on IQ or brain function, long-term study shows ~ NBC News

4-13-26
www.nbcnews.com/health/kids-...

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Blueroot Health Expands Voluntary Allergy Alert on Undeclared Egg, Hazelnut, and Soy in Vital Nutrients Aller-C Dietary Supplements April 10, 2026 — Middletown, CT — Blueroot Health of Middletown, Connecticut is expanding its voluntary recall of its Vital Nutrients Aller-C dietary supplements due to the potential to contain undecl...

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📢 UPDATE:
The initial recall, which included lots 25E04-A and 25E04-B, has been EXPANDED to include ALL product made from lot 25E04.

4-10-26
www.fda.gov/safety/recal...

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Chocolate recalled because it contains erectile dysfunction drug Nalpac is voluntarily recalling DTF Sexual Chocolate it purchased and resold because it has been found to contain sildenafil and tadalafil.  Sildenafil and tadalafil are the active ingredients in the...

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⚠️ Recall: Contains UNDECLARED Rx Drugs
SILDENAFIL + TADALAFIL E.D. meds

Nalpac
DTF SEXUAL CHOCOLATE
UPC 757817783069

Sold at: Adult Retail Stores + Online

4-7-26
www.foodsafetynews.com/2026/04/choc...

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Orange Flavored Addall SR Shot and Capsules Contain DMAA The FDA is warning consumers in a public health alert to avoid Orange Flavored Addall SR Shot and Addall XL Capsules because they contain DMAA and DMHA,

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⚠️ FDA Public Health Alert: UNDECLARED + UNLAWFUL INGREDIENTS
Banned stimulants: phenibut, DMAA, DMHA

ZMB Enterprises
*Orange Flavored ADDALL SR SHOT
*ADDALL XL CAPSULES

Dist: 🇺🇲 NATIONWIDE

4-11-26
foodpoisoningbulletin.com/2026/orange-...

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Good Brain Tonic Recalled For Possible Botulism Contamination Good Brain Tonic is being recalled for possible botulism contamination, according to a Consumer Alert published by the New York Department of Agriculture

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⚠️ Recall: Possible CLOSTRIDIUM BOTULINUM Contamination

Liquid Blenz Corporation
*GOOD BRAIN TONIC - 16 oz + 32 oz bottles

Sold Retail + Online: 🇺🇲 NATIONWIDE

4-8-26
foodpoisoningbulletin.com/2026/good-br...

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A product photo of Blaine Labs Revitaderm Wound Care Gel - Benzalkonium Chloride, in the 1 ounce and 3 ounce sizes. Applicator tip designs may vary. Revitaderm is one of two Blaine Labs topical products that are implicated in a recall for microbial contamination of Lysinibacillus fusiformis.

Please use the hyperlink in this post to access the FDA Recall page which includes the pertinent information including Lot numbers, EXP dates and company contact information.

A product photo of Blaine Labs Revitaderm Wound Care Gel - Benzalkonium Chloride, in the 1 ounce and 3 ounce sizes. Applicator tip designs may vary. Revitaderm is one of two Blaine Labs topical products that are implicated in a recall for microbial contamination of Lysinibacillus fusiformis. Please use the hyperlink in this post to access the FDA Recall page which includes the pertinent information including Lot numbers, EXP dates and company contact information.

A product photo of Trifluent Pharma Tridergel Wound Care Gel - Benzalkonium Chloride, in the 1 ounce and 3 ounce sizes. Applicator tip designs may vary. Tridergel is one of two Blaine Labs topical products that are implicated in a recall for microbial contamination of Lysinibacillus fusiformis.

**The FDA Recall page doesn't mention Trifluent Pharma which is the manufacturer name featured on this product. Confusing. Blaine Labs appears to manufacture a Tridergel product, but I could not find any alternate product photos.

Please use the hyperlink in this post to access the FDA Recall page which includes the pertinent information including Lot numbers, EXP dates and company contact information.

A product photo of Trifluent Pharma Tridergel Wound Care Gel - Benzalkonium Chloride, in the 1 ounce and 3 ounce sizes. Applicator tip designs may vary. Tridergel is one of two Blaine Labs topical products that are implicated in a recall for microbial contamination of Lysinibacillus fusiformis. **The FDA Recall page doesn't mention Trifluent Pharma which is the manufacturer name featured on this product. Confusing. Blaine Labs appears to manufacture a Tridergel product, but I could not find any alternate product photos. Please use the hyperlink in this post to access the FDA Recall page which includes the pertinent information including Lot numbers, EXP dates and company contact information.

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⚠️ Recall: Microbial Contamination - LYSINIBACILLUS FUSIFORMIS

Blaine Labs Inc
*REVITADERM WOUND CARE ANTISEPTIC GEL - 1 oz + 3 oz
*TRIDERGEL WOUND CARE - 1 oz

Dist to HEALTHCARE PROVIDERS (doctor's offices): 🇺🇲 NATIONWIDE

4-8-26
www.fda.gov/safety/recal...

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Millions of eye drops recalled nationwide amid safety fears According to the FDA, a “lack of assurance of sterility” is the reason behind the action, which impacts a range of products.

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⚠️ Class II Recall: LACK OF ASSURANCE OF STERILITY

K.C. Pharmaceuticals
OVER-THE-COUNTER (OTC) EYE DROP PRODUCTS
*8 Varieties

📢 Sold under multiple BRAND NAMES + thru MAJOR retailers
+ various OTHER OUTLETS

Dist: 🇺🇲 NATIONWIDE

4-3-26
www.newsweek.com/millions-eye...

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A photo of the packaging and accompanying literature for Kian Pee Wan capsules which are implicated  in a recall by Ebay seller: Aphreseller, for containing the undeclared medications, dexamethasone (a corticosteroid) and cyproheptadine (a prescription antihistamine), which combined with other ingredients, create a new, unapproved drug, for which safety and efficacy have not been established, and are therefore, subject to recall.

Please use the hyperlink in this post to access the FDA Recall page with the pertinent information including product photos and company contact information.

A photo of the packaging and accompanying literature for Kian Pee Wan capsules which are implicated in a recall by Ebay seller: Aphreseller, for containing the undeclared medications, dexamethasone (a corticosteroid) and cyproheptadine (a prescription antihistamine), which combined with other ingredients, create a new, unapproved drug, for which safety and efficacy have not been established, and are therefore, subject to recall. Please use the hyperlink in this post to access the FDA Recall page with the pertinent information including product photos and company contact information.

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⚠️ Recall: Undeclared Drug Ingredients -
DEXAMETHASONE + CYPROHEPTADINE

Aphreseller (eBay ID)
KIAN PEE WAN capsules - for appetite + weight gain

Sold on EBAY.com: 🇺🇸 NATIONWIDE

4-1-26
www.fda.gov/safety/recal...

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*What's in Your Fish Oil Pill? ~ Consumer Reports

🦋 Follow: @consumerreports.org

4-2-26

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A graphic of the label for one of the Lots of Vital Nutrients Aller-C 200 count, which is part of a recall by Blueroot Health for the undeclared  allergens of egg, hazelnut and soy.

Please use the hyperlink in this post to access the FDA Recall page which includes the pertinent information including more label photos, UPC codes, Lot Numbers, expiration dates and company contact information.

A graphic of the label for one of the Lots of Vital Nutrients Aller-C 200 count, which is part of a recall by Blueroot Health for the undeclared allergens of egg, hazelnut and soy. Please use the hyperlink in this post to access the FDA Recall page which includes the pertinent information including more label photos, UPC codes, Lot Numbers, expiration dates and company contact information.

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⚠️ Recall: Undeclared Allergen - EGG, HAZELNUT, SOY

Blueroot Health
VITAL NUTRIENTS ALLER-C
*100 ct
*200 ct

Dist via VitalNutrients + other Online Retailers: 🇺🇸 NATIONWIDE

3-27-26
www.fda.gov/safety/recal...

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FDA issues chocolate recall, warning it poses a specific danger to men Anyone who has consumed the "sex chocolate" has been advised to get in touch with Gear Isle's customer team.

#USfoodrecalls #USfoodsafety #USdrugrecalls #USdrugsafety 📎👆

✅ Check similar recalls in this feed

*FDA issues chocolate recall, warning it poses a specific danger to men
~ Newsweek

📢 Good info on the serious risks of unknowingly ingesting these meds

3-27-26
www.newsweek.com/fda-issues-c...

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A product photo of a pouch of Gold Lion Aphrodisiac Chocolate Sachet which is 1 of 2 such products implicated in a recall by Gear Isle for containing the undeclared prescription erectile dysfunction medications sildenafil and tadalafil.
It is potentially  hazardous  to unknowingly  consume medication that could interact with other meds and cause adverse reactions.

Please use the hyperlink in this post to access the FDA Recall page for all the pertinent information including the UPC code, Lot code and expiration date.

A product photo of a pouch of Gold Lion Aphrodisiac Chocolate Sachet which is 1 of 2 such products implicated in a recall by Gear Isle for containing the undeclared prescription erectile dysfunction medications sildenafil and tadalafil. It is potentially hazardous to unknowingly consume medication that could interact with other meds and cause adverse reactions. Please use the hyperlink in this post to access the FDA Recall page for all the pertinent information including the UPC code, Lot code and expiration date.

A product photo of a pouch of ilum Sex Chocolate Male Sexual Enhancement Booster which is 1 of 2 such products implicated in a recall by Gear Isle for containing the undeclared prescription erectile dysfunction medications sildenafil and tadalafil.
It is potentially  hazardous  to unknowingly  consume medication that could interact with other meds and cause adverse reactions.

Please use the hyperlink in this post to access the FDA Recall page for all the pertinent information including the UPC code, Lot code and expiration date.

A product photo of a pouch of ilum Sex Chocolate Male Sexual Enhancement Booster which is 1 of 2 such products implicated in a recall by Gear Isle for containing the undeclared prescription erectile dysfunction medications sildenafil and tadalafil. It is potentially hazardous to unknowingly consume medication that could interact with other meds and cause adverse reactions. Please use the hyperlink in this post to access the FDA Recall page for all the pertinent information including the UPC code, Lot code and expiration date.

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⚠️ Recall: Contains UNDECLARED Rx Drugs
SILDEAFIL + TADALAFIL E.D. meds

Gear Isle
*GOLD LION APHRODISIAC CHOCOLATE SACHET
*ilum SEX CHOCOLATE MALE SEXUAL ENHANCEMENT BOOSTER

Dist via INTERNET: NATIONWIDE

3-26-26
www.fda.gov/safety/recal...

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9 Ibuprofen Interactions: What To Avoid When You’re Taking Ibuprofen Understanding Ibuprofen Interactions for Safe Usage Ibuprofen is one of the most widely used over-the-counter pain relievers and anti-inflammatory medications. While it’s effective for headaches, musc...

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*9 IBUPROFEN INTERACTIONS: What to Avoid When You're Taking Ibuprofen
~ Doctronic - (medically reviewed by Alan Lucks MD)

12-18-25
www.doctronic.ai/blog/9-ibupr...

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A product photo of an outer carton for Ultra Advanc3 which is implicated in an FDA Advisory to consumers not to purchase or use Ultra Advanc3 and Ultra Advanc3 Gold, which are promoted and sold for joint pain, because testing confirmed the undeclared medications: dexamethasone, diclofenac + methocarbamol which are not listed on the product labels.

Please use the hyperlink in this post to access the FDA Medication Health Fraud Notification page for these products with the pertinent information, including the hazards associated with unknowingly consuming medications that can interact with other medicines and cause adverse reactions.

A product photo of an outer carton for Ultra Advanc3 which is implicated in an FDA Advisory to consumers not to purchase or use Ultra Advanc3 and Ultra Advanc3 Gold, which are promoted and sold for joint pain, because testing confirmed the undeclared medications: dexamethasone, diclofenac + methocarbamol which are not listed on the product labels. Please use the hyperlink in this post to access the FDA Medication Health Fraud Notification page for these products with the pertinent information, including the hazards associated with unknowingly consuming medications that can interact with other medicines and cause adverse reactions.

A product photo of an outer carton for Ultra Advanc3 Gold which is implicated in an FDA Advisory to consumers not to purchase or use Ultra Advanc3 and Ultra Advanc3 Gold, which are promoted and sold for joint pain, because testing confirmed the undeclared medications: dexamethasone, diclofenac + methocarbamol which are not listed on the product labels.

Please use the hyperlink in this post to access the FDA Medication Health Fraud Notification page for these products with the pertinent information, including the hazards associated with unknowingly consuming medications that can interact with other medicines and cause adverse reactions.

A product photo of an outer carton for Ultra Advanc3 Gold which is implicated in an FDA Advisory to consumers not to purchase or use Ultra Advanc3 and Ultra Advanc3 Gold, which are promoted and sold for joint pain, because testing confirmed the undeclared medications: dexamethasone, diclofenac + methocarbamol which are not listed on the product labels. Please use the hyperlink in this post to access the FDA Medication Health Fraud Notification page for these products with the pertinent information, including the hazards associated with unknowingly consuming medications that can interact with other medicines and cause adverse reactions.

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⚠️ FDA Advisory: CONTAINS UNDECLARED MEDICATIONS -
Dexamethasone, Diclofenac, Methocarbamol

ULTRA ADVANC3 + ULTRA ADVANC3 GOLD

Sold on AMAZON, NATURISTAREX.COM + other retailers

2-26-26
www.fda.gov/drugs/medica...

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Multivitamin with Fluoride Chewable Tablets Grape Flavor recalled due to Vitamin D Subpotent , Symptoms: , Details: Winder Laboratories, LLC has initiated a voluntary recall of its Multivitamin with Fluoride Chewable Tablets, Grape Flavor, due to subpotency of

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⚠️ Recall: SUBPOTENCY- VITAMIN D

Winder Laboratories LLC
MULTIVITAMIN with FLOURIDE CHEWABLE TABLETS- Grape Flavor
*0.25 mg - 100 ct
*1 mg - 100 ct

Dist: 🇺🇸 23 STATES + HI 🇵🇷 PR

3-18-26
iwaspoisoned.com/food-recall/...

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A photo of an outer carton for Cardinal Health brand Large Alcohol Prep Pads (70% isopropyl alcohol) which are implicated in an urgent recall for microbial contamination of Paenibacillus phoenicis, which is potentially hazardous for at-risk populations.

Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including link to a table with all of the affected lot numbers, more product photos and company contact information.

A photo of an outer carton for Cardinal Health brand Large Alcohol Prep Pads (70% isopropyl alcohol) which are implicated in an urgent recall for microbial contamination of Paenibacillus phoenicis, which is potentially hazardous for at-risk populations. Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including link to a table with all of the affected lot numbers, more product photos and company contact information.

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⚠️ Recall: Microbial Contamination - PAENIBACILLUS PHOENICIS

Cardinal Health
*LARGE ALCOHOL PREP PADS (70% isopropyl alcohol)

Dist @ consumer level: 🇺🇸 U.S. 🇵🇷 PR 🇯🇵 JAPAN

3-20-26
www.fda.gov/safety/recal...

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Nearly 90,000 Bottles of Children’s Ibuprofen Were Just Recalled—Here’s Why What parents need to know.

#USdrugrecalls #USdrugsafety #ChildSafety #MOMsky

⚠️ Class II Recall: Foreign Material Contamination-
GEL-LIKE MASS + BLACK PARTICLES

Strides Pharma
*100-milligram CHILDREN'S IBUPROFEN ORAL SUSPENSION 4 fl oz bottle

Dist: 🇺🇸 NATIONWIDE

3-20-26
www.goodhousekeeping.com/health/a7080...

4 3 0 0

#USfoodrecalls #USfoodsafety #USdrugrecalls #USdrugsafety 📎👆

📢 Check your medicine cabinets!

bsky.app/profile/yoka...

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#USfoodrecalls #USfoodsafety #USdrugrecalls #USdrugsafety 📎👆

📢 Check your medicine cabinets!

bsky.app/profile/yoka...

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Why Not and Live It Up Moringa Salmonella Outbreak Grows The Why Not and Live It Up moringa Salmonella outbreak has grown, with at least 65 people in 28 states sick and 14 hospitalizations. That is an increase

#USfoodrecalls #USfoodsafety #USdrugrecalls #USdrugsafety

*'Why Not' and 'Live It Up' Moringa Salmonella Outbreak Grows
~ FPB

3-9-26 📎👇
foodpoisoningbulletin.com/2026/why-not...

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#USfoodrecalls #USfoodsafety #USdrugrecalls #USdrugsafety

📢 2-27-26 SIMILAR RECALL 📎👆

bsky.app/profile/yoka...

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📢 2-25-26 SIMILAR RECALL 📎👆

bsky.app/profile/yoka...

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A product photo of Boner Bears Honey 15 serving package, along with a 
15G serving pouch on top. It is implicated in a recall by Pure Vitamins and Natural Supplements LLC of some of its Sexual Enhancement products for containing undeclared prescription medications. FDA analysis confirmed that Boner Bears Honey contains Sildenafil + Tadalafil which are prescribed for erectile dysfunction.

It is potentially hazardous to unknowingly  consume medication that could interact with other meds and cause adverse reactions.

Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including more product photos, UPC numbers, expiration & best by dates and company contact information

A product photo of Boner Bears Honey 15 serving package, along with a 15G serving pouch on top. It is implicated in a recall by Pure Vitamins and Natural Supplements LLC of some of its Sexual Enhancement products for containing undeclared prescription medications. FDA analysis confirmed that Boner Bears Honey contains Sildenafil + Tadalafil which are prescribed for erectile dysfunction. It is potentially hazardous to unknowingly consume medication that could interact with other meds and cause adverse reactions. Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including more product photos, UPC numbers, expiration & best by dates and company contact information

A product photo of Red Bull Extreme 15 serving package, along with a 
15G serving pouch on top. It is implicated in a recall by Pure Vitamins and Natural Supplements LLC of some of its Sexual Enhancement products for containing undeclared prescription medications. FDA analysis confirmed that Red Bull Extreme and another product: Blue Bull Extreme contain Sildenafil which is prescribed for erectile dysfunction.

It is potentially hazardous to unknowingly  consume medication that could interact with other meds and cause adverse reactions.

Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including more product photos, UPC numbers, expiration & best by dates and company contact information

A product photo of Red Bull Extreme 15 serving package, along with a 15G serving pouch on top. It is implicated in a recall by Pure Vitamins and Natural Supplements LLC of some of its Sexual Enhancement products for containing undeclared prescription medications. FDA analysis confirmed that Red Bull Extreme and another product: Blue Bull Extreme contain Sildenafil which is prescribed for erectile dysfunction. It is potentially hazardous to unknowingly consume medication that could interact with other meds and cause adverse reactions. Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including more product photos, UPC numbers, expiration & best by dates and company contact information

#USfoodrecalls #USfoodsafety #USdrugrecalls #USdrugsafety

⚠️ Recall: Contains UNDECLARED Rx Drugs-
SILDENAFIL + TADALAFIL E.D. meds

Pure Vitamins & Natural Supplements LLC
Sexual Enhancement Honey Products
*BONER BEAR HONEY
*RED BULL EXTREME
*BLUE BULL EXTREME

3-14-26
www.fda.gov/safety/recal...

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A product photo of a container of Primal Herbs Volume Herbal Supplement, which is implicated in an urgent recall for containing the undeclared prescription medication Sildenafil for erectile dysfunction. 
It is potentially hazardous to unknowingly consume medication that could interact with other meds and cause adverse reactions.

Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including the sales window in which the affected product was sold and company contact information.

A product photo of a container of Primal Herbs Volume Herbal Supplement, which is implicated in an urgent recall for containing the undeclared prescription medication Sildenafil for erectile dysfunction. It is potentially hazardous to unknowingly consume medication that could interact with other meds and cause adverse reactions. Please use the hyperlink in this post to access the FDA Recall page for all of the pertinent information including the sales window in which the affected product was sold and company contact information.

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⚠️ Recall: UNDECLARED Rx Drug - SILDENAFIL (E.D. med)

Primal Supplements Group LLC
PRIMAL HERBS - VOLUME

Sold via primalherbs.com from 7/2/25 - 9/19/25

3-11-26
www.fda.gov/safety/recal...

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Safety Alert FDA analysis has determined that certain dietary supplements labeled as tejocote (Crataegus mexicana) root are adulterated because they were tested and found to be substituted withyellow oleander (Cas...

#USdrugrecalls #USdrugsafety

⚠️ Supplements / Products with TEJOCOTE ROOT or BRAZIL SEED

📢 FDA list of supplement products that testing has shown contain poisonous YELLOW OLEANDER, instead of the stated tejocote root or Brazil seed.

Up-to-date as of 3-11-26
www.fda.gov/food/alerts-...

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