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Safety Reports: Drugs

Updated: February 5, 2024 7:03 PM

Arize male enhancement capsules - recalled due to undeclared Nortadalafil, USA

9 months ago •source fda.gov • details

Recall notice

"Today The World” is voluntarily recalling one lot of Arize Herbal Dietary Supplement capsules to the consumer level. FDA analysis has found the products to contain undeclared Nortadalafil. The product was distributed online via their website in the USA. To date, no adverse events have been reported.… See more

#recall #drugs #unitedstates

Arize male enhancement capsules - recalled due to undeclared Nortadalafil photo #1

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TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence, USA

9 months ago •source fda.gov • details

Recall notice

Insight Pharmaceuticals is voluntarily recalling two lots of TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid to the consumer level due to elevated levels of benzene. The affected TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid lots were distributed nationwide in the United States through… See more

#recall #drugs #unitedstates

TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence photo #1

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Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tianeptine, USA

9 months ago •source fda.gov • details

Recall notice

Neptune Resources, LLC issues a voluntary recall of Neptune's Fix Elixir, Neptune's Fix Extra Strength Elixir, and Neptune's Fix Tablets Products Due to the Presence of Tianeptine. The products were distributed nationwide in the USA to wholesale and retail customers. Neptune Resources LLC's distribution channels have not… See more

#recall #drugs #unitedstates

Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tianeptine photo #1

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Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package, USA

9 months ago •source fda.gov • details

Recall notice

Azurity Pharmaceuticals, Inc. is voluntarily recalling one lot (F230169A) of Zenzedi® CII (dextroamphetamine sulfate tablets, USP) 30 mg to the consumer level. The product is being recalled due to a report from a pharmacist in Nebraska who opened a bottle of Zenzedi® 30 mg tablets and found… See more

#recall #drugs #unitedstates

Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package photo #1

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Robitussin Cough syrups - recalled due to microbial contamination, USA

9 months ago •source fda.gov • details

Recall notice

Haleon is voluntarily recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult to the consumer level. The product is being recalled due to microbial contamination. To date, Haleon has not received any reports of adverse events related to this… See more

#recall #drugs #unitedstates

Robitussin Cough syrups - recalled due to microbial contamination photo #1

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Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns, USA

9 months ago •source fda.gov • details

Recall notice

Kilitch Healthcare India Limited is issuing an amendment in the last Nationwide press release dated November 13, 2023 issued for nationwide recall of various eye drops. These products were distributed nationwide in the USA to wholesalers, retailers, and via the product distributor, Velocity Pharma LLC.

There are… See more

#recall #drugs #unitedstates

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Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose, Canada

10 months ago •source recalls-rappels.canada.ca • details

Recall notice

Teva Canada Ltd. is recalling a single lot of its Pediatrix Acetaminophen Oral Solution for children due to an increased risk of overdose. The product was distributed nationwide in Canada. The product is available without a prescription and is used to relieve mild to moderate pain and… See more

#drugs #recall #canada

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Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency, USA

10 months ago •source fda.gov • details

Recall notice

Leiters Health is voluntarily recalling 33 lots of products to the user level. The recalled batches of vancomycin IV bags, phenylephrine IV bags, and fentanyl IV bags are being recalled due to the potential for superpotency because they may contain twice the labeled amount of drug. The… See more

#recall #drugs #unitedstates

Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency photo #1

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Semaglutide medications Marketed for Type 2 Diabetes or Weight Loss - Warning and risks, USA

10 months ago •source fda.gov • details

Outbreak

WARNING
On December 21, 2023, the FDA published a warning to consumers, healthcare providers, and pharmacists to not use counterfeit Ozempic (semaglutide) injection 1 milligram, which has entered the U.S. drug supply chain. This counterfeit product is labeled with lot number NAR0074 and serial number 430834149057. FDA… See more

#ozempic #drugs #unitedstates

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Hospira Sodium bicarbonate & Atropine sulfate injections - recalled due to the presence of glass particulate matter, USA

10 months ago •source fda.gov • details

Recall notice

Hospira, Inc., a Pfizer company, is voluntarily recalling the lots listed in the table below of 4.2% Sodium Bicarbonate Injection, USP ABBOJECT® Glass Syringe, 5 mEq/10 mL; 8.4% Sodium Bicarbonate Injection, USP Lifeshield® ABBOJECT® Glass Syringe, 50 mEq/50 mL; and Atropine Sulfate Injection, USP Lifeshield® ABBOJECT® Glass… See more

#recall #drugs #unitedstates

Hospira Sodium bicarbonate & Atropine sulfate injections - recalled due to the presence of glass particulate matter photo #1

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Safety Reports: Drugs

Arize male enhancement capsules - recalled due to undeclared Nortadalafil, USA

TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence, USA

Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tianeptine, USA

Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package, USA

Robitussin Cough syrups - recalled due to microbial contamination, USA

Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns, USA

Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose, Canada

Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency, USA

Semaglutide medications Marketed for Type 2 Diabetes or Weight Loss - Warning and risks, USA

Hospira Sodium bicarbonate & Atropine sulfate injections - recalled due to the presence of glass particulate matter, USA

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