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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.
Freshpoint Central Florida, Inc.'s Cranberry Chicken Salad Wedge 4.5 oz packages are affected. The hazard is an undeclared egg allergen, posing a risk to consumers with egg allergy. Consumers with egg allergy should not eat the product and should discard or return it.
Sweet Sensi Elevated Edibles Hybrid Gum Drops Passion Guava Kush 140mg THC, batch 1811, sold in 10-count and 30-count pouches nationwide are affected. The product contains Staphylococcus aureus, which can cause food poisoning in anyone who eats it. Consumers should not eat the product and should discard it or return it to the place of purchase.
Pepsico Inc is recalling 28 oz. Gatorade Lemon Lime, Lemon Lime Zero, Orange, and Orange Zero drinks. The drinks contain undeclared Yellow No. 5 and/or Yellow No. 6, which can cause allergic reactions in sensitive consumers. Consumers should check their bottles and return or discard any affected product.
Saint Francis Apizza LLC is recalling its frozen Mushroom and Onion Pizza in 17 oz vacuum-sealed packages. The product contains undeclared soybean oil and soy lecithin, which can cause serious reactions in people with soy allergy. Consumers should not eat the pizza and should return it to the place of purchase or throw it away.
LEASA Living Alfalfa Sprouts, sold by LEASA Industries Co., Inc., are recalled. The sprouts may be contaminated with E. coli, posing a risk to anyone who purchased them in Florida or New Hampshire. Consumers should not eat them and should discard or return the product.
J K Patisserie & Bakery LLC's Lemon Blueberry Loaf in a cardboard box is recalled because it contains undeclared soybean oil and soy lecithin. People with soy allergy are at risk of a serious reaction. Consumers should not eat the product and should return it to the store or contact the firm.
A&P Creations biQ-FEL, a 16.9 fluid ounce liquid supplement distributed by Biofel, is recalled. The product contains undeclared Sildenafil and Tadalafil, posing a health risk to consumers who use it. Consumers should stop using the product and return it to the place of purchase or discard it.
Saint Francis Apizza Frozen Supreme Pizza, 17 ounces, is recalled. The pizza contains undeclared soy, posing a risk to people with soy allergy. Consumers should check the UPC and return or throw away the product.
Berlin Seeds Alfalfa Sprouting Seeds, sold in 1/4 lb., 1/2 lb., 1 lb., 5 lb. resealable bags and 50 lb. woven poly bags, are recalled. The seeds may contain E. coli and/or Salmonella, posing a risk to anyone who eats them. Consumers should not eat the seeds and should return or discard them.
The Better Bakehouse Snack Company is recalling Donutful Chocolate Dipped Vanilla Cake Donuts sold in 7.05oz/10ct cartons with UPC 850041392103. The donuts contain undeclared milk, posing a risk to people with milk allergy or sensitivity. Consumers should not eat the product and should discard it or return it to the place of purchase.
The recall affects bettergoods Lemon Alfredo Fettuccine, distributed by Walmart Inc. The product may contain Listeria monocytogenes, which poses a health risk to anyone who eats it. Consumers should not eat it and must return it to the store or discard it.
The recall affects Mezzetta Golden Greek Peperoncini Medium Heat 32 fluid ounce jars from G L Mezzetta Inc. The jars may contain foreign objects, specifically mice, posing a safety risk to consumers who purchased them. Consumers should not eat the product and should return it to the store or throw it away.
Saint Francis Apizza frozen cheese pizza, 17 ounces, is recalled. The pizza contains undeclared soy, posing a risk to people with soy allergy. Consumers should not eat it and should return or throw it away.
J K Patisserie & Bakery LLC croissants in cardboard boxes are recalled. The croissants contain undeclared egg, posing a risk to people with egg allergy. Consumers should not eat them and should return or discard the product.
WinCo Foods Salsa Bean Dip Express Tray and 16-inch catering tray are affected. The trays contain recalled peperoncini due to a pest issue, posing a contamination risk to consumers. Consumers should not eat the recalled products.
LEASA Industries Co., Inc. is recalling LEASA Alfalfa Sprouts in 6-ounce plastic clamshell containers. The sprouts may be contaminated with E.coli, posing a health risk to consumers in Florida and New Hampshire. Consumers should not eat them and should return or discard the product.
A&P Creations X10 Natural Enhancement Supplement, distributed by Natur Fuel, is recalled. The product contains undeclared Sildenafil and Tadalafil, posing a risk to consumers nationwide who purchased it. Consumers should stop using the supplement and return it to the place of purchase.
J K Patisserie & Bakery LLC is recalling its Chocolate Chip Cookies in a cardboard box because soy is not declared on the label. People with a soy allergy who eat these cookies could have a serious or life-threatening reaction. Consumers should not eat the cookies and should return them to the store or throw them away.
Saint Francis Apizza LLC is recalling Saint Francis Apizza Frozen Pepperoni Pizza in 17 oz vacuum-sealed packages. The product contains undeclared soy allergen, posing a risk to people with soy allergy. Consumers with soy allergy should not eat this pizza.
Queso Palmita brand Pastel de Queso (Cheese Pie), a frozen product in 1.2 lb packages, is recalled. The product contains undeclared milk, posing a risk to people with milk allergies or sensitivities. Consumers who bought it in Texas should not eat it and should return or discard the product.
The Conqueror is recalling its Avengers Infinity Gauntlet medal, a gold medal with colorful gems sold in a Marvel Avengers package. The high-powered magnets can detach and, if swallowed by children, cause intestinal perforation, blockage, blood poisoning, or death. Consumers should stop using the recalled medals and contact The Conqueror for a refund.
Snow Peak is recalling its Takibi propane fireplace inserts and lava rocks, model ST-332-US. The lava rocks can ignite and explode when heated, posing burn and fire hazards that can cause serious injury or death to consumers. Consumers should stop using the recalled product immediately.
Romorgniz six-drawer dressers in white and black are recalled. The dressers can tip over and entrap children if not anchored, posing serious injury or death. Consumers should stop using the recalled dressers immediately.
Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.