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Safety Reports: Drugs

Updated:

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to Due to Potential Lack of Sterility Assurance., USA

8 months ago •source fda.gov • details

Recall notice

Company name: Brassica Pharma Pvt. Ltd.
Brand name: Multiple brands
Product recalled: Eye ointment products
Reason of the recall: Due to Potential Lack of Sterility Assurance.
FDA Recall date: February 26, 2024
Recall details: Company Announcement FOR IMMEDIATE RELEASE – 12 February, 2024 – Thane, Maharashtra, India,… See more

#recall #drugs #unitedstates

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

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

10 months ago •source fda.gov • details

Recall notice

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

Americaine Benzocaine Topical Anesthetic Spray - recalled due to Presence of benzene photo #1

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

10 months ago •source fda.gov • details

Recall notice

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

Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial - recalled due to Presence of Glass Particulate Matter photo #1

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

11 months ago •source fda.gov • details

Recall notice

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

InvaGen Pharmaceuticals Inc. Vigabatrin for Oral Solution - recalled due to malfunction photo #1

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

11 months ago •source fda.gov • details

Recall notice

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

Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil photo #1

Novartis Sandimmune Oral Solution - recalled due to due to crystallization formation, USA

11 months ago •source fda.gov • details

Recall notice

Novartis is conducting a voluntary nationwide recall at the consumer level of two lots of its Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL in the US due to crystal formation observed in some bottles, which could potentially result in incorrect dosing. The issue was identified… See more

#recall #drugs #unitedstates

Novartis Sandimmune Oral Solution - recalled due to due to crystallization formation photo #1

TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder - recalled due to presence of benzene, USA

11 months ago •source fda.gov • details

Recall notice

Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company (“Insight”), is voluntarily recalling two lots of TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder to the consumer level. A recent review by our manufacturer and their third-party lab found that samples from two lots of the… See more

#recall #drugs #unitedstates

TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder - recalled due to the presence of benzene photo #1
1

Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination, USA

11 months ago •source fda.gov • details

Recall notice

Bayer is voluntarily recalling one lot of Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles to the consumer/user level. The product is being recalled due to microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing. It was distributed to wholesale distributors and… See more

#recall #drugs #unitedstates

Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination photo #1

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