1278 alerts recorded, refreshed every six hours. Filter by source or category.
Fresenius Kabi USA is recalling Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL, 20 mL vials. The vials contain glass particles, posing a risk to patients who receive the injection. Consumers should stop using the product and contact their healthcare provider or pharmacist for guidance.
Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 175 mcg, in 90-count and 1000-count bottles. The tablets are subpotent, meaning they contain less active ingredient than expected, which can affect patients who take this thyroid medication. Consumers should check their bottles for the affected NDC numbers listed in the recall.
Church & Dwight Co. Inc. is recalling Zicam Cold Remedy Medicated Nasal Swabs with Cooling Menthol & Eucalyptus, 20 single-use swabs per carton. The swabs may be contaminated because microbiological testing showed out-of-limit results, posing a risk to consumers nationwide. Consumers should stop using the recalled swabs and follow the firm's recall instructions for return or disposal.
Accord Healthcare is recalling Levothyroxine Sodium Tablets, USP, 150 mcg, in 1000-count bottles. The tablets may be subpotent, meaning patients may not receive the full dose, posing a risk to those with thyroid conditions. Consumers who have this medication should stop using it and contact their pharmacy or healthcare provider for a replacement.
Mallinckrodt Hospital Products Inc. is recalling Acthar Gel (repository corticotropin injection) 5 mL multiple-dose vials. The vials may contain glass and stopper particles, posing a risk to patients who receive the injection. Consumers should stop using the recalled product and contact their healthcare provider or pharmacy for guidance.
Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 75 mcg, 1000-count bottles. The tablets are subpotent, posing a risk to patients who take this thyroid medication. Consumers should stop using the recalled bottles and consult their pharmacist or doctor.
Accord Healthcare is recalling Levothyroxine Sodium Tablets, USP, 300 mcg (0.3 mg), 90-count bottles. The tablets may be subpotent, meaning patients taking them may not receive the full dose. Consumers should check their bottles and contact their pharmacist or healthcare provider for guidance.
Lupin Pharmaceuticals Inc. is recalling Clobetasol Propionate Cream USP, 0.05%, 60 g tubes, prescription only. The cream failed content uniformity specifications, affecting patients who use the product. Consumers should stop using the recalled tubes and return them to the pharmacy.
Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 137 mcg, in 90-count and 1000-count bottles. The tablets may be subpotent, meaning patients may not receive the full intended dose of thyroid hormone. Consumers should stop using the affected product and contact their pharmacist or healthcare provider for instructions.
Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 25 mcg, 1000-count bottles. The tablets may be subpotent, meaning they contain less active ingredient than expected, which can affect patients who rely on this thyroid medication. Consumers should stop using the recalled bottles and return them to their pharmacy or contact their doctor for a replacement.
Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 125 mcg, in 1000-count bottles, distributed nationwide in the United States. The tablets may be subpotent, meaning patients may not receive the full dose of their thyroid medication, posing a health risk to those who take it. Consumers should stop using the affected bottles and return them to the pharmacy or contact their healthcare provider for guidance.
Accord Healthcare is recalling Levothyroxine Sodium Tablets, USP, 50 mcg, in 1000-count bottles. The tablets may be subpotent, meaning patients may not receive the full dose of thyroid hormone. Consumers should stop taking the recalled bottles, check the NDC 16729-448-17, and return them to their pharmacy for a replacement.
Hikma Pharmaceuticals is recalling its Ramipril Capsules USP, 10 mg, sold in 100 and 500 capsule bottles. The capsules contain an impurity called dicyclohexylurea that fails degradation specifications, posing a risk to patients taking them. Consumers should stop using the recalled capsules and contact their pharmacist or the manufacturer for instructions.
Accord Healthcare, Inc. is recalling Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg) in 90-count and 1000-count bottles. The tablets may be subpotent, meaning they contain less active ingredient than expected, which can affect patients who rely on this thyroid medication. Consumers should check their bottle's NDC and lot number and contact their pharmacist or doctor for guidance.
Botticelli Foods, LLC is recalling bettergoods brand Pistachio Nut Butter, 6.7 oz, UPC 194346207961. The product may be contaminated with Salmonella, which can cause serious illness in consumers who eat it. Consumers should not eat it and should discard it or return it to the place of purchase.
The recalled product is Mehadrin Chocolate Leben, 6 oz cups with UPC 070784023144, distributed by Upstate Niagara Cooperative in New Jersey. The product may have been improperly pasteurized, posing a health risk to consumers who eat it. Consumers should not consume the product and should return or discard it.
Sirna & Sons Produce is recalling its PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, product number 55255. The jalapeno peppers may be contaminated with Salmonella Javiana, which can cause serious illness in consumers who eat them, and were distributed for food service use in Ohio and Pennsylvania. Consumers and food service operators should not use the product and should return or discard it.
Byron White Formulas A-L Complex Herbal Supplement, 1.0 fl. oz./30 mL, by Byron White Formulas, Inc. is recalled. The label does not declare walnuts, posing a risk to consumers with a walnut allergy. Consumers should stop using the product and return it to the place of purchase or discard it.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Tangerine, 6-count 2.5 ounce packages with UPC 041548612041. The bars may contain glass pieces, posing a risk to anyone who eats them. Consumers should not eat the product and should discard it or return it to the store.
Byron White Formulas, Inc. is recalling Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL. The label does not declare walnuts, posing a risk to consumers with nut allergies. Consumers should not consume this product if they have a walnut allergy.
Jaime's Foods ATX, LLC Jalapeno Ranch in 16 oz glass jars is recalled. The product contains undeclared egg, posing a risk to people with egg allergy. Consumers should not eat it and should return or discard the product.
The recall affects KHONG GUAN (HQ) Black and White Glutinous Rice Balls with Black Sesame Filling, 14.1 oz, product of China. The product has undeclared peanuts, which is dangerous for people with peanut allergies. Consumers who bought this product should not eat it and should follow the recall instructions.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars in Strawberry, Pineapple, Grape, and Tangerine flavors, 24-count 2.5 ounce packages with UPC 041548816678. The frozen fruit bars may contain glass pieces, posing a risk of injury to consumers who eat them. Consumers should check their freezers for the recalled UPC, not eat the product, and return it to the store or throw it away.
Horizon Organic chocolate milk 1% in 8-ounce 12-count and 18-count Tetra Pak cartons is recalled. The milk may be spoiled, posing a risk to anyone who drinks it. Consumers should not drink the product and should return or discard it.
Lidl US is recalling ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating and Apricot Filling. The cookies have undeclared wheat, soy, milk, eggs, and coconut, which can cause allergic reactions in sensitive people. Consumers should not eat them and should return them to the store or throw them away.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Black Cherry, 6 bars, 2.5 ounce, UPC 041548000121. The fruit bars may contain glass pieces, posing a risk to consumers in many states. Consumers should not eat the recalled product and should discard or return it.
Lidl US is recalling ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with coconut sprinkles. The cookies contain undeclared wheat, soy, milk, eggs, and coconut, posing a risk to people with allergies. Consumers should not eat the product and should return it to the store or discard it.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Strawberry, 6-count 2.5 ounce packages with UPC 041548610047. The frozen fruit bars may contain glass pieces, posing a risk to consumers who eat them. Consumers should check the UPC and not eat the affected product.
Marketside Tomato Bisque Soup Kit with cheese croutons and white cheddar cheese, ready to heat, 14 oz, is recalled. The soup may contain Listeria monocytogenes, posing a serious infection risk to consumers, especially pregnant women, the elderly, and those with weak immune systems. Consumers who bought the product in the listed states should not eat it and should discard it or return it to the store for a refund.
ZMB Enterprises recalled Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement. The product contains 1,4-DMAA, Phenylethylamine, and Phenibut, which pose health risks to consumers who purchased it online. Consumers should stop using the product and discard it or return it to the place of purchase.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Grape, 6-count 2.5 ounce packages with UPC 041548244044. The bars may contain glass pieces, posing a risk to consumers who eat them. Consumers should not eat the recalled bars and should return or discard them.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bar Watermelon, 6-count 2.5 ounce bars with UPC 041548413624. The frozen bars may contain glass pieces, posing a risk of injury to consumers who purchased them in the listed states. Consumers should not eat the product and should discard it or return it to the place of purchase.
The recalled product is Byron White Formulas A-FNG Herbal Supplement 1.0 fl. oz./30 mL. The label does not declare walnuts in English, posing a risk to people with walnut allergies. Consumers should stop using the product and return it to the place of purchase or discard it.
The recall affects KHONG GUAN (HQ) Glutinous Rice Balls with Black Sesame Filling, 14.1 oz, UPC 6908791000053. The product contains undeclared peanuts, posing a risk to people with peanut allergies. Consumers should not eat the product and should return it to the store or discard it.
H & U Inc. dba Sun Noodle is recalling Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base ramen noodle kits. The Soba sauce packet contains undeclared fish (bonito, sardine, mackerel), posing a risk to consumers with fish allergies. Consumers should not eat the product and should return it to the store or discard it.
The recall involves Mainstays Nine-Drawer Fabric Dressers sold by Walmart. The dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can cause serious injury or death to children. Consumers should immediately stop using the recalled dressers and contact Walmart for a full refund.
Steelite electric pressure washers, model AZ6041VC, sold on Amazon by Longer 3D are recalled. The washers lack a ground-fault circuit-interrupter and adequate power cord, posing shock and electrocution hazards to users. Consumers should stop using the recalled pressure washers immediately.
The recalled product is the YERYORK-branded electric pressure washer, model YE-006, sold on Amazon. The pressure washers lack a ground-fault circuit-interrupter and an adequate-length power cord, posing serious shock and electrocution risks to consumers. Consumers should stop using the recalled pressure washers.
The recalled product is the Chillife 5-in-1 Montessori Baby Toy Set, sold on Amazon by Chillife Official. The pull string teething toy has silicone strings that are too small and long, which can reach the back of a child's throat and cause choking or death. Consumers must immediately stop using the recalled toy.
Little Loves & Co. recalled youth daywear sets and boy short sets with waist drawstrings in sizes 12/18 months through youth 9/10. The drawstrings can catch on objects and cause death or serious injury from entrapment to children wearing them. Consumers should stop using the recalled clothing and contact Little Loves & Co. for a refund or replacement.
Kmaier infant walkers, model RV001, are recalled. The walkers can fit through standard doorways and fail to stop at step edges, posing a deadly fall hazard to infants. Consumers should stop using them and contact Kmaier for instructions.
The recalled product is the HABA Rainbow Rattle Grasping and Teething Toy, item number 2012261001, batch code 0925. The glued knot on the elastic cord can untie, allowing young children to access small wooden and plastic pieces, posing a risk of serious injury or death from choking and ingestion. Consumers should immediately stop using the toy and keep it away from children.
Excel Industries is recalling accessory LED Light Kits used on Hustler or BigDog ride-on mowers. The light bars can overheat or produce flames, posing a serious fire hazard to consumers. Consumers should stop using the kits and contact Excel Industries for a free replacement or repair.
Diamond Wipes International is recalling MD Wipe Outz Numbing Tattoo Wipes, sold in foil packets. The wipes contain lidocaine and are not in child-resistant packaging, posing a risk of serious injury or death if young children ingest them. Consumers should stop using the recalled wipes and contact Diamond Wipes International for a refund or replacement.
The recall affects Cuisinart metal wire bristle grill brushes, including models previously and newly recalled. Small wire bristles can detach and stick to grills or food, posing an ingestion hazard that can cause serious internal injuries requiring surgery. Consumers should stop using these brushes and contact Conair for a refund or replacement.
AudioLineOut is recalling its Studio Six Headphone Amplifiers, model ST6, in black or silver. When used with aftermarket metal base tubes, the bare metal can become electrified, posing a risk of serious injury or death from electrocution to users. Consumers must stop using the amplifiers with aftermarket metal base tubes.
Dentsply Sirona Capsule Mixer Model No. 5546068 is recalled. The unit may cause electrical discharge when unplugged, exposing users to shock. Consumers should stop using the mixer and contact Dentsply Sirona.
The recalled product is the Getinge Y Sensor Module, model 6693662, used in SERVO-U and SERVO-N continuous ventilator systems for facility use. The module skipped electrical safety and functional tests during production, exposing patients and staff to potential device failure. Consumers should contact Maquet Critical Care for instructions on returning or replacing the affected module.
Arrowhead DE LLC's Arrow-LOK Implant is affected. The implant may have reduced sterility assurance due to a missing gamma radiation dose audit, which could lead to patient infection in those undergoing toe fixation procedures. Consumers should follow the voluntary recall initiated by the firm.
Tobii Dynavox is recalling its TD Navio Maxi Speech Generating Device, model 1000799. Damaged battery mounting tabs can let the battery move and cause an internal short circuit, leading to localized heating and gas venting for users. Consumers should contact Tobii Dynavox for instructions.
Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.