262 recalls tagged with “lithium battery”.
Tampa Maid Foods recalled 776 cases of Panko Style Breaded Butterfly Shrimp due to potential Cesium-137 contamination. The product was distributed to 16 states. Consumers should not eat the shrimp and should contact the company for refunds or replacements.
Exactech recalled 11,542 Equinoxe reverse shoulder humeral liners worldwide after finding the articular surface position outside labeling specifications. The recall covers several REF numbers and UDIs and is active as of 2025. Healthcare providers were advised to stop using affected liners and follow manufacturer instructions.
Exactech recalled 61,334 Equinoxe reverse shoulder humeral liners sold worldwide after finding the articular surface position outside labeling dimensions. The recall covers REF 320-38-00, REF 320-38-03, REF 320-42-00, and REF 320-42-03. Healthcare providers and patients should stop using the devices immediately and follow recall instructions distributed by email.
Werner recalls 2 ladder models sold nationwide after reports of locking mechanism jams. The recall affects Werner 20' ALMP-20IAA and 24' ALMP-24IAA Multi-Max Pro multi-purpose ladders. Consumers should stop using these ladders and contact Werner for a full refund.
ESR HaloLock wireless power banks, distributed by Waymeet, are recalled. The lithium-ion battery can overheat and ignite, creating a fire and burn hazard. Stop using the recalled power banks and contact Waymeet for a full refund.
Philips North America recalls 210 CT systems worldwide after reports that the patient support couch may descend unexpectedly to the lowest position following a replacement. Philips issued a recall dated 2025-08-13 with active status. The recall number is Z-2598-2025. Stop using immediately and follow manufacturer instructions.
Fresh & Ready Foods recalled 233 Spanish Club Ciabatta sandwiches sold to 15 California locations after discovering undeclared wheat and milk allergens. The recall is Class I and the hazard is an undisclosed allergen on ready-to-eat sandwiches. Consumers should not eat the sandwiches and should contact Fresh & Ready Foods for refunds or replacements by email.
Novartis Manufacturing NV and Sandoz Inc recall ciprofloxacin 0.3% and dexamethasone 0.1% otic suspension after temperature abuse. The recall affects one consignee in California. Consumers and health care providers should stop using the product immediately and follow guidance from Sandoz or a healthcare provider.
Penner Patient Care recalls 190 Bathing Spa devices nationwide after discovering the units lack a unique device identifier. The issue involves missing UDI on the device. Stop using the device immediately and follow the recall instructions.
Penner Patient Care recalled 25 Penner Pacific Bathing Spas nationwide after confirming the device does not bear a unique device identifier. The missing UDI impedes traceability and oversight. Stop using the device and follow the manufacturer’s recall instructions.
Penner Patient Care, Inc. recalled 21 Penner Pacific Bathing Spa units distributed nationwide in the United States after discovering the devices do not bear a unique device identifier. The missing UDI hinders traceability for adverse events and recalls. Consumers should stop using the devices and contact Penner Patient Care for instructions.
Baker's Authority LLC recalls 78 units of Three Seed Mix, 5 lb bags, distributed to multiple states. The recall follows labeling errors that fail to list sesame as an ingredient. Consumers who purchased this product should not consume it and should email Baker's Authority LLC for refund or replacement information.
Lannett Company, Inc. recalls 8,544 bottles of Lisdexamfetamine Dimesylate 40 mg capsules distributed nationwide. A labeling mix-up may have placed 30 mg and 40 mg strengths in mislabeled bottles. Healthcare providers and patients should stop use and contact the company for guidance.
Glenmark Pharmaceuticals Inc. USA recalls theophylline extended-release 400 mg tablets after dissolution test failures. The recall covers 22,656 bottles distributed nationwide in the United States. Consumers should stop using the product and contact Glenmark for guidance.
Breckenridge Pharmaceutical recalls duloxetine delayed-release capsules due to CGMP deviations raising N-nitroso-duloxetine impurity above interim limit. The bottles were distributed to Arizona, Indiana and New Jersey. Consumers should stop using the product and contact their healthcare provider for guidance.
Glenmark Pharmaceuticals Inc. recalls 44,328 bottles of Carvedilol tablets, 3.125 mg, distributed nationwide in the USA. The impurity N-nitroso carvedilol I exceeds the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark for guidance.
Petmate recalled Pet Zone Laser Pointer & LED Ball toys sold exclusively at Menards. The recall date is August 7, 2025. The products contain six preinstalled button cell batteries and pose an ingestion hazard if the battery compartment is breached. Consumers should stop using the recalled toys and contact Petmate for a full refund.
Monica Vinader recalls select 14k yellow gold mini heart bracelets, necklaces and stud earrings due to high cadmium levels. The recalled jewelry was manufactured in October and November 2024. Consumers should stop wearing the jewelry immediately and contact Monica Vinader for a replacement or refund.
Fieldsheer Apparel Technologies is recalling heated socks MWMS07, MWWS07 and MWMS05. The recall covers socks sold with two lithium-ion battery packs and a charging cable. Consumers should stop using the product and contact Fieldsheer for a refund or replacement.
Deale International recalls Altafit AF28 smartwatches sold by HSN after reports of overheating charging pads. The recall cites a risk of serious burn injury and fire. Consumers should stop charging the watch immediately and contact Deale International for a free replacement.