378 recalls tagged with “kitchen”.
Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.
GE Medical Systems recalled 7,302 AW Server models worldwide, including 1,381 units in the U.S., after identifying a security vulnerability that could expose patient data. The defect could allow a malicious actor to compromise confidentiality, integrity and availability of information. Healthcare providers should stop using the devices immediately and follow manufacturer instructions for recall.
Pacific Coast Producers recalled 1,836 cases of Pears Halves in Pear Juice from Concentrate distributed by Walmart. The product may be contaminated with lead, a heavy metal hazard. Consumers should not eat this product and should contact Pacific Coast Producers for a refund or replacement by telephone.
American Contract Systems recalled 32,433 medical convenience kits nationwide after finding re-gassed devices from EO sterilization. The recall affects five product lines with UDI-DI codes and Lot numbers. The re-gassing process has not been validated for multiple sterilization cycles, calling into question product safety and effectiveness. Health providers and patients should stop using these kit
Pacific Coast Producers recalled 609 cases of Fruit Cocktail in 15 oz cans distributed by Wegmans Food Markets over lead contamination concerns. The recall cites potential contamination with lead. Consumers who purchased the product should not consume it and should contact Pacific Coast Producers for a refund or replacement.
ONE FROZEN recalled 57,240 bags of Good and Gather Southwest-Style Burrito Bowl Blend sold nationwide after discovering undeclared shrimp. The product may contain shellfish due to cross-contact risk in a facility that also handles shellfish and other allergens. Consumers should not eat the product and should contact ONE FROZEN for a refund or replacement.
The FDA confirms a nationwide recall of Zydus Lifesciences Chlorpromazine Hydrochloride tablets 200 mg (NDC 70710-1133-1) distributed by Zydus Pharmaceuticals USA. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above acceptable intake. Consumers and healthcare providers should stop using the product immediately and contact the distributor for guidance.
Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride tablets, 25 mg, 100-count bottles distributed nationwide by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above the acceptable intake limit. Stop using the product and contact your healthcare provider or Zydus Pharmaceuticals (USA) Inc. for
Endico Potatoes Inc recalled 280 cases of Endico brand Frozen Mixed Vegetables distributed to retailers in New York, New Jersey, Connecticut, Florida, Pennsylvania, Maryland and the District of Columbia. The product may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact Endico Potatoes for refunds or replacements.
Endico Potatoes Inc. recalled 335 cases of Endico brand PEAS & CARROTS distributed to seven states after authorities flagged Listeria monocytogenes. The product should not be eaten. Consumers should contact Endico Potatoes for refund or replacement information. The recall was active as of Sept. 3, 2025.
New Spirit Naturals recalls 79 units of Meal In A Glass protein powder sold directly to consumers online over an undeclared milk allergen. The recall is active as of the enforcement report dated 2026. Consumers who purchased the product should not consume it and contact the company for refund or replacement.
Philips Medical Systems Nederland recalled 2,317 Allura Xper FD10 imaging systems worldwide, including 497 in the United States. The BIOS battery may deplete faster than expected, causing the startup process to halt with no user alerts. Hospitals should stop using the devices and await manufacturer instructions.
The FlexLab X System Potassium Test System was recalled by Inpeco S.A. on 2025-09-03 after the FDA identified an unvalidated hemolysis, icterus, and lipemia function in its Sample Integrity Module. The recall affects US distribution to California and New York. Stop using immediately and follow manufacturer instructions.
Philips Medical Systems Nederland B.V. recalled 585 units of the Allura Xper FD10/10 diagnostic system globally, including 145 in the United States, after reports that the BIOS battery can deplete faster than expected and halt system startup. The recall covers models 722005, 722011, and 722027. Healthcare facilities should stop using the device and follow manufacturer instructions for remediation.
Philips Medical Systems Nederland B.V. recalls 313 Allura Centron devices with model 722400 worldwide after a BIOS battery drains too quickly. The issue can halt the system start-up with no user warning. The recall was issued September 3, 2025 and remains active as of October 8, 2025. Consumers should contact Philips or their healthcare provider for instructions.
Major Pharmaceuticals recalls sulfamethoxazole and trimethoprim 800 mg/160 mg double-strength tablets sold nationwide. A specific lot of packaging coil used in production was found to contain a microorganism in the packaging area, though no microorganism was detected on the tablets. Consumers should stop using the product and follow guidance from Major Pharmaceuticals or their healthcare provider.
LeMaitre Vascular recalled 28 Artegraft Collagen Vascular Grafts distributed nationwide in 17 states. The grafts use bovine carotid arteries sourced from a supplier not reviewed by the appropriate regulatory authority. Patients and healthcare providers should stop using the device immediately and contact LeMaitre Vascular for instructions.
ICF Factory recalled 12 pints of Vanilla G. Nutt Ice Cream sold in New York after an undeclared almond allergen was detected. The product may contain almond not listed in ingredients. Consumers should not eat it and contact ICF Factory for refund or replacement information.
ImaCor recalls 45 CLT-010 miniaturized TEE probes nationwide in five states after a production assembly error risks reversed articulation. The device is used with ImaCor model ZHH and Mobile Ultrasound. Stop using the device immediately and follow the manufacturer’s recall instructions.
Northeast Scientific recalled 141 units of the NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter nationwide in the United States. The device may have breaches in the sterile barrier packaging that could compromise sterility. Hospitals and patients should stop using the device immediately and await instructions from Northeast Scientific Inc. or their clinicians.