171 alerts recorded, refreshed every six hours. Filter by source or category.
Houston Rx LLC is recalling Tirzepatide/Niacinamide 2mL vials (40 MG per Vial) Inj 20mg/2mg/mL. The vials lack assurance of sterility, exposing patients nationwide to potential infection risk. Consumers should stop using the recalled vials.
Zydus Pharmaceuticals is recalling Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial. The injection fails impurity and degradation specifications, posing a risk to patients who receive it. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacy for guidance.
American Health Packaging is recalling Metoclopramide Tablets, USP, 5 mg, 100-count bottles. The bottles may contain foreign tablets or capsules, which poses a risk to patients taking this medication. Consumers should stop using the product and contact their pharmacist or American Health Packaging for instructions.
Teva Pharmaceuticals is recalling Metoclopramide Tablets, USP, 5 mg, in 100 and 500 tablet bottles. The tablets may contain foreign tablets or capsules, posing a risk to consumers nationwide. Consumers should stop using the recalled tablets and return them to the pharmacy.
Houston RX LLC is recalling Sermorelin, 1 mg/mL, 10 ml vial, sterile injectable solution. The lack of process control may cause the product to be non-sterile or incorrectly dosed, posing a risk to patients who inject it. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacy for instructions.
Apothecary Pharma LLC is recalling Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vials, prescription only. The vials lack assurance of sterility, posing a risk of infection to patients who receive the injection nationwide. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacy for instructions.
K.C. Pharmaceuticals, Inc. is recalling sterile eye drops redness relief sold under brands including Leader, Discount Drug Mart, Equaline, Colirio Ojo de Aguila, Clear Eyes, Equate, Walgreens, and Xpect. The products lack assurance of sterility, posing a risk of infection to consumers who use them. Consumers should stop using the recalled eye drops and return them to the place of purchase or discard them.
Carolina Infusion, LLC is recalling Sermorelin Acetate 1 mg/mL injectable, packaged in single-use dosage syringes and distributed nationwide. The product lacks assurance of sterility, exposing patients who receive the injectable to a potential risk of infection. Consumers should stop using the recalled product and contact their healthcare provider or pharmacy for guidance.
Carolina Infusion LLC is recalling semaglutide 3 mg/mL injectable syringes, 8 x 0.1 mL, distributed nationwide. The product lacks assurance of sterility, exposing patients to risk of infection. Consumers should stop using the recalled syringes and contact Carolina Infusion LLC for instructions.
Carolina Infusion, LLC is recalling its Semaglutide/Cyanocobalamin 3/2 mg/mL injectable, packaged in single-use dosage syringes. The product lacks assurance of sterility, exposing patients to potential infection. Consumers should stop using the recalled product and contact their healthcare provider or pharmacy.
K.C. Pharmaceuticals, Inc. is recalling sterile eye drops AC (tetrahydrozoline HCl 0.05%, zinc sulfate 0.25%) sold under brands Equaline, Good Sense, H.E.B, QC-Quality Choice, and TopCare. The products lack assurance of sterility, posing a risk of infection to consumers who use them. Consumers should stop using the recalled eye drops and return them to the place of purchase.
Taro Pharmaceuticals is recalling Tretinoin Cream USP, 0.05%, 45g tubes. The cream failed impurities and degradation specifications, exposing patients nationwide to a potential health risk. Consumers should stop using the recalled product and follow the firm's recall instructions.
Carolina Infusion, LLC is recalling its Semaglutide/Cyanocobalamin 9/2 mg/mL injectable, packaged in single-use dosage syringes. The product lacks assurance of sterility, exposing patients who use the injectable to potential infection. Consumers should stop using the recalled syringes and contact their healthcare provider or Carolina Infusion for guidance.
K.C. Pharmaceuticals is recalling Artificial Tears Sterile Lubricant Eye Drops sold under brands such as Best Choice, Leader, Walgreens, and Kroger. The drops may lack sterility, exposing users to risk of eye infection. Consumers should stop using the product and return it to the store or discard it.
Carolina Infusion, LLC is recalling tirzepatide 26 mg/mL injectable in single-use syringes. The product may not be sterile because it was made with bacteriostatic water and certain processing equipment, exposing patients nationwide to infection risk. Consumers should stop using the recalled syringes and contact their prescriber or the firm for return instructions.
BioSpectra, Inc. is recalling its Biospectra Tris/Tromethamine, USP, GMP, API Grade, NDC 64173-101-25, made at 100 Majestic Way, Bangor, PA. The product failed stability specifications, which may affect its quality or potency, exposing consumers to potential health risks. Consumers should stop using the recalled product and return or dispose of it as directed.
Carolina Infusion, LLC is recalling TIRZEPATIDE/CYANOCOBALAMIN 76/2 MG/ML injectable, packaged in single-use dosage syringes. The product lacks assurance of sterility, exposing patients to potential infection. Consumers should stop using the product and contact their healthcare provider for guidance.
The recall affects K.C. Pharmaceuticals' Maximum Redness Relief sterile eye drops sold under brands including exchange select, Harris Teeter, Mike Red Eye Drops, up & up, TopCare health, and Walgreens. The hazard is a lack of assurance of sterility, exposing consumers who use these eye drops to potential infection. Consumers should stop using the recalled eye drops and return them to the place of purchase.
Sun Pharmaceutical Industries is recalling Tretinoin Cream USP, 0.05%, 20g, a prescription cream made by Taro Pharmaceuticals and distributed nationwide. The cream failed impurities and degradation specifications, which could affect its quality and safety for patients using it. Consumers should stop using the recalled tubes and return them to their pharmacy or contact their doctor for a replacement.
Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 64/2 mg/mL injectable in single-use syringes. The product may not be sterile, posing a risk of infection to patients who use it. Consumers should stop using the product and contact their healthcare provider or the company for instructions.
K.C. Pharmaceuticals, Inc. is recalling Sterile High Performance Ultra Lubricating Eye Drops sold under Leader, exchange select, Good Sense, and Walgreens brands. The eye drops lack assurance of sterility, posing a risk to consumers who use them. Consumers should stop using the recalled eye drops.
Carolina Infusion, LLC's Tirzepatide/Cyanocobalamin 85/2 mg/mL injectable, packaged in single-use syringes, is affected. The product lacks assurance of sterility due to formulation with bacteriostatic water and processing equipment, exposing patients nationwide to potential infection. Consumers should follow the recall instructions from Carolina Infusion or the FDA.
Sun Pharmaceutical Industries is recalling Tretinoin Cream USP, 0.05%, 45 g tubes sold under the Northstar Rx LLC brand. The cream failed impurity and degradation specifications, exposing users nationwide to a potential quality risk. Consumers should stop using the recalled tubes and follow the firm's instructions for return or disposal.
Carolina Infusion, LLC is recalling Tri-MIX (PAPAV/PHENTO/ALPROS), 30/2/20, injectable syringes. The products lack assurance of sterility, posing a risk of infection to patients nationwide. Consumers should stop using the product and contact their healthcare provider or pharmacy for guidance.
Preferred Pharmaceuticals is recalling Lidocaine Ointment USP 5% in 50 g jars. The product failed content uniformity, so patients may receive inconsistent amounts of the drug. Consumers should stop using the recalled ointment and return it to where they purchased it.
Apothecary Pharma LLC is recalling Tirzepatide Injection, 18mg/mL, 4 mL sterile multi-dose vials, sold nationwide. The vials lack assurance of sterility, exposing patients to potential infection. Consumers should stop using the product and contact Apothecary Pharma for instructions.
Carolina Infusion, LLC is recalling Tri-MIX (PAPAV/PHENTO/ALPROS), 30/1/40, an injectable packaged in single-use dosage syringes. The product may lack sterility assurance due to processing equipment, exposing patients nationwide to infection risk. Consumers should stop using the syringes and contact their healthcare provider or pharmacy for further instructions.
K.C. Pharmaceuticals is recalling tetrahydrozoline HCl 0.05% redness reliever eye drops sold under brands including Best Choice, Equate, Walgreens, and Kroger. The products may lack sterility assurance, posing a risk of infection to consumers who use them. Consumers should stop using the drops and return them to the place of purchase or discard them.
The recall covers IMAAVY (nipocalimab-aahu) Injection, 300 mg/1.62 mL, a prescription drug from Janssen Biotech. The hazard is particulate matter in the vials, which could harm patients receiving the infusion. Consumers should stop using the recalled product and contact their healthcare provider or pharmacy.
Carolina Infusion, LLC is recalling Tri-MIX (papaverine/phentolamine/alprostadil) 30/2/40 single-use dosage syringes. The syringes lack assurance of sterility, posing a risk of infection to patients nationwide. Consumers should stop using the recalled syringes and return them to Carolina Infusion, LLC.
Cipla USA is recalling Fosfomycin Tromethamine Granules for Oral Solution, 3 grams, single-dose sachets, a prescription antibiotic. The product fails impurities and degradation specifications, posing a risk to patients who take it. Consumers should stop using the recalled sachets and contact their pharmacist or doctor for guidance.
K.C. Pharmaceuticals is recalling Advanced Relief sterile eye drops sold under brands including Leader, Equaline, GoodSense, H.E.B, and TopCare. The products may lack sterility assurance, posing a risk of eye infection to users. Consumers should stop using the recalled eye drops and follow the recall notice.
Carolina Infusion, LLC is recalling Tri-MIX (papaverine/phentolamine/alprostadil) 30/1/60 injectable syringes. The syringes may not be sterile because of processing equipment, posing a risk of infection to patients. Patients should stop using the product and contact their healthcare provider or pharmacy for a replacement.
Carolina Infusion, LLC is recalling Tri-MIX (papaverine/phentolamine/alprostadil) 30/1/10 injectable syringes. The syringes may lack sterility assurance, posing a risk of infection to patients who receive them. Consumers should stop using the product and contact their healthcare provider or pharmacy for guidance.
Carolina Infusion, LLC is recalling Tri-MIX (papaverine/phentolamine/alprostadil) 30/1/20 injectable syringes. The product may not be sterile due to processing equipment issues, posing a risk of infection to patients nationwide. Consumers should stop using the product and return it to the pharmacy.
The affected product is Tirzepatide/Cyanocobalamin 26/2 mg/mL injectable in single-use syringes from Carolina Infusion, LLC. The hazard is a lack of assurance of sterility from the formulation and processing equipment, exposing patients nationwide to possible infection. Consumers should contact their healthcare provider or pharmacy for guidance about this voluntary recall.
Carolina Infusion, LLC is recalling QUAD-MIX (papaverine, phentolamine, alprostadil, tropicamide) injectable syringes. The syringes may not be sterile due to processing equipment issues, posing infection risk to patients. Consumers should stop using the product and contact their healthcare provider or pharmacy for guidance.
K.C. Pharmaceuticals is recalling its Sterile Lubricant Dry Eye Relief Eye Drops sold under multiple brands including Leader, Crocodile Tears, and TopCare. The eye drops lack assurance of sterility, posing a risk of infection to consumers who use them. Consumers should stop using the recalled product and return it to the place of purchase.
Ajanta Pharma USA Inc. is recalling Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottles, distributed nationwide in the US. The tablets failed dissolution specifications, meaning they may not release the drug properly, posing a risk to patients who take this prescription medication. Consumers should stop using the recalled tablets and contact their pharmacist or doctor for a replacement or guidance.
Par Health USA, LLC is recalling Buprenorphine Hydrochloride Injection 0.3 mg/mL single-dose vials, manufactured for Endo USA. The product may crystallize, posing a hazard to patients receiving the injection nationwide. Consumers should contact their healthcare provider or pharmacist for instructions.
The recalled product is Benzoyl Peroxide Wash, USP, 5%, 5 FL OZ, distributed by Rugby Laboratories. The hazard is microbial contamination of the topical product, exposing consumers in Illinois. Consumers should stop using the product and return it to the place of purchase.
Apotex Corp. is recalling Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottles, distributed nationwide. The tablets failed dissolution specifications, meaning they may not release the drug properly, posing a risk to patients who take this prescription. Consumers should stop using the recalled lot and contact their pharmacist or doctor for a replacement or guidance.
TerSera Therapeutics LLC is recalling Zoladex (goserelin) implant 3.6 mg single-use syringes. The product was exposed to non-temperature-controlled conditions for 25.5 hours, potentially affecting patients nationwide. Consumers should stop using the product and contact their healthcare provider or pharmacy for instructions.
The recall affects Aurolab Trust FOCUS PI Hypromellose 0.7% Formula sterile eye drops in 10 mL vials. The hazard is lack of assurance of sterility, which exposes users to risk of infection. Consumers must stop using the recalled eye drops and contact the firm or return them as directed.
Amneal Pharmaceuticals is recalling its Estradiol Gel, 0.1%, 0.25 mg, sold in 30-packet cartons nationwide. The packets may be empty or partially full, exposing patients to an incorrect dose of this prescription hormone gel. Consumers should stop using the affected product and contact Amneal Pharmaceuticals for further instructions.
Rugby Laboratories' Benzoyl Peroxide Wash, USP, 10%, in 5 oz and 8.5 oz bottles, is recalled. The topical product may be contaminated with microbes, posing a risk to consumers using it. Consumers should stop using the recalled wash and return or discard it.
Menow Sunscreen Pressed Powder SPF35 PA+++ from Shantou Qiwei Industry Co. Ltd is recalled. The product has manufacturing practice deviations, exposing users in California to potential health risks. Consumers should stop using it and return or discard it as instructed.
Reliable-1 Laboratories Lubricating Tears sterile eye drops in 0.5 FL OZ bottles are affected. The products lack assurance of sterility, posing a risk to consumers who use them. Consumers should stop using the recalled bottles and follow the recall instructions.
Insight Pharmaceuticals LLC is recalling Clear Eyes Redness Relief Lubricant/Redness Reliever Eye Drops, 0.5 fl oz bottles, distributed nationwide. The eye drops may not be sterile, posing a risk of infection to consumers who use them. Consumers should stop using the recalled product and return or discard it.
Walgreens Lubricant Eye Drops, carboxymethylcellulose sodium 0.5%, sterile 0.5 oz bottles are affected. The hazard is lack of assurance of sterility, exposing users to potential eye infection. Consumers should stop using the product and return or discard it.
Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.