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Drugs

Updated: December 26, 2023 4:01 PM

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

4 months ago •source www.fda.gov

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 #us

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

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

4 months ago •source www.fda.gov

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 #us

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

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

4 months ago •source www.fda.gov

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 #us

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

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

4 months ago •source www.fda.gov

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 #us

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

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

5 months ago •source www.fda.gov

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 #us

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

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

5 months ago •source www.fda.gov

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 #us

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

5 months ago •source www.fda.gov

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 #us

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

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

5 months ago •source www.fda.gov

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 #us

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Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil, USA

5 months ago •source www.fda.gov

Recall notice

Noah’s Wholesale, LLC is voluntarily recalling one lot of rock# 03032021, exp:12/2027, 1200 mg/capsule, to the consumer level. FDA analysis has found the product to be tainted with Sildenafil. The product was distributed locally through convenience stores and some island jobbers (small wholesale distributors to retail). Noah’s … See More

#dietarysupplements #recall #drugs #us

Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil photo #1

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KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instability, USA

5 months ago •source www.fda.gov

Recall notice

KinderFarms, LLC is voluntarily recalling all lots of KinderMed Infants’ Pain & Fever (oral suspension) and KinderMed Kids’ Pain & Fever (oral suspension) to the retail and consumer level. These products are being voluntarily recalled due to acetaminophen instability. These products are available nationwide in drug/pharmacy, supermarkets, … See More

#recall #drugs #us

KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instability photo #1

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Drugs

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

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

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

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

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

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

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

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

Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil, USA

KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instability, USA

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