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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Robitussin Cough syrups - recalled due to microbial contamination, USA

1 year ago •source fda.gov • details

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

Recalls Robitussin Cough syrups - recalled due to microbial contamination Haleon is voluntarily recalling ei... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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

Recalls Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns Kilitch He... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source recalls-rappels.canada.ca • details

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

Recalls Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose Teva Canada Ltd.... photo #1
87   Comments Comment

Recall notice

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

2 years ago •source fda.gov • details

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

Recalls Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug... photo #1
313   Comments Comment

Outbreak

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

2 years ago •source fda.gov • details

####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

Outbreak Semaglutide medications Marketed for Type 2 Diabetes or Weight Loss - Warning and risks WARNING On D... photo #1
314   Comments Comment

Recall notice

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

2 years ago •source fda.gov • details

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

#drugs #recall #unitedstates

Recalls Hospira Sodium bicarbonate & Atropine sulfate injections - recalled due to the presence of glass par... photo #1
312   Comments Comment

Recall notice

Americaine Benzocaine Topical Anesthetic Spray - recalled due to Presence of benzene, USA

2 years ago •source fda.gov • details

Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company ("Insight"), is voluntarily recalling one lot of Americaine® 20% Benzocaine Topical Anesthetic Spray to the consumer level. While benzene is not an ingredient in any Americaine® 20% Benzocaine Topical Anesthetic Spray products, a recent review by our manufacturer and… See more

#recall #drugs #unitedstates

Recalls Americaine Benzocaine Topical Anesthetic Spray - recalled due to Presence of benzene Insight Pharmac... photo #1
312   Comments Comment

Recall notice

Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial - recalled due to Presence of Glass Particulate Matter, USA

2 years ago •source fda.gov • details

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Bleomycin for Injection, USP 15 units Single Dose ONCO-TAIN™ Glass Fliptop Vial, to the user level. The recall was initiated due to a confirmed customer report for the presence of glass particulate within a single vial.… See more

#recall #drugs #unitedstates

Recalls Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial - recalled due to Pr... photo #1
312   Comments Comment

Recall notice

InvaGen Pharmaceuticals Inc. Vigabatrin for Oral Solution - recalled due to malfunction, USA

2 years ago •source fda.gov • details

Cipla Limited today announced that its wholly-owned subsidiary, InvaGen Pharmaceuticals Inc. is voluntarily recalling one lot of Vigabatrin for Oral Solution, USP 500mg, to the consumer level. Vigabatrin for Oral Solution, USP 500 mg has been found to have seal integrity issues allowing for powder leakage from… See more

#recall #drugs #unitedstates

Recalls InvaGen Pharmaceuticals Inc. Vigabatrin for Oral Solution - recalled due to malfunction Cipla Limite... photo #1
312   Comments Comment

Recall notice

Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil, USA

2 years ago •source fda.gov • details

Meta Herbal is voluntarily recalling 500 blister packs of Magnum XXL 9800 2000 mg per capsule, to the consumer level. The products have been found to be tainted with Sildenafil. Products containing sildenafil cannot be marketed as dietary supplements. Magnum XXL 9800 capsules is an unapproved new… See more

#drugs #recall #amazon #unitedstates

Recalls Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil Meta Herbal is volun... photo #1
312   Comments Comment

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