153 recalls tagged with “holiday product”.
King Harvest Roasted Red Pepper Hummus, distributed in Oregon and Washington by Pacific Coast Fresh Co, is recalled. The recall cites foreign material aluminum pieces found in 10 oz and 17 oz tubs. Consumers should not eat the product and should contact Pacific Coast Fresh Co for a refund or replacement.
Pacific Coast Fresh Co. recalled 760 King Harvest Jalapeno Hummus containers distributed in Oregon and Washington. Aluminum pieces were found as a foreign material in the product. Consumers should not consume this hummus and should contact the company for refund or replacement.
Imu-Tek Animal Health recalled 1,003 bottles of Colostrum-5 sold through various retailers in 30 states after determining the product may be under-processed. The under-processing could render the product unsafe. Consumers should not consume the product and should contact Imu-Tek Animal Health for refund or replacement.
Yiruikeji2024 recalled magnetic chess games on February 24, 2026, due to ingestion hazards. The games contain loose magnets that can pose serious health risks to children. Consumers should stop using the product and seek a refund immediately.
Made Fresh Salads recalled 557 five‑pound tubs of Walnut Raisin Cream Cheese distributed in New York after identifying a potential Listeria monocytogenes contamination. The product is a Walnut Raisin Cream Cheese in a 5‑pound white plastic tub. Consumers who bought this product should not consume it and should contact Made Fresh Salads Inc for refunds or replacements by telephone.
Navajo Manufacturing recalled 28,457 Handy Solutions Neck & Shoulders Heating Pads sold nationwide through Multiple Retailers. The defect allows overheating if the pad is folded or placed under the body, and the high limit device may fail to shut off. Stop use and contact Navajo Manufacturing for instructions.
Medline Industries recalled 651,789 ENFIT G-TUBE connectors (ENFIT1010GC) sold worldwide, including the United States and Canada. The connectors were not manufactured to required dimensional specifications and may not seal properly with ENFit-style devices, which could lead to leakage. Healthcare facilities and patients should stop using this device immediately and follow recall instructions from
Olympus Corporation of the Americas recalled 3,354 units of the OER-Pro endoscope reprocessor on February 12, 2026. MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the device immediately and follow the manufacturer’s recall instructions.
Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.
Burlington Medical, LLC recalled 103 leg wrap devices distributed worldwide through multiple retailers. The recall cites attenuation degradation over time that could shorten the devices' lifespan. Healthcare providers and patients should stop using them immediately and follow the manufacturer's recall instructions.
International Life Sciences recalled Artelon FlexBand Plus augmentation devices after endotoxin testing failures. The recall affects devices with REF 41054 and REF 41057 distributed worldwide. Patients and healthcare providers must stop using the devices immediately and follow manufacturer instructions for recall return.
Dresbe LED Christmas Headbands are recalled in 2026 after a battery ingestion hazard was identified. The recall covers a two-pack set labeled HB-052. Stop using the headbands and contact Dresbe for a full refund.
Olympus Corporation of the Americas recalls 1,276 boxes of MAJ-1218 Single Use Biopsy Valve distributed nationwide to healthcare facilities. The device risks rubber fragment detachment during use. Stop using the device and follow the recall instructions from Olympus or your healthcare provider.
Abiomed recalled 179 Impella RP devices worldwide after a differential pressure sensor may drift. The fault can cause sensor values to drift, potentially affecting patient care. Stop using the device immediately and follow the recall instructions, including contacting Abiomed or your healthcare provider.
Mangalm LLC recalled 40 cases of Tops GOLD Stuffed Red Chilli Pickle, 31.74 oz cans, distributed in California, Nevada, Oregon, Utah and Washington. The recall is due to potential adulteration with erucic acid from mustard oil. Consumers should not consume this product and should contact Mangalm LLC by email for a refund or replacement.
A worldwide distribution recall covers 74 GEM PAK cartridges for the GEM Premier 5000. The issue involves PCSND errors during warm-up that can trigger ejection of GEM PAKs and may delay results. Institutions should follow recall instructions from Instrumentation Laboratory and notify healthcare teams immediately.
Instrumentation Laboratory recalled 27 GEM Premier 5000 PAK cartridges sold to healthcare facilities worldwide after reports of PCSND errors during warm-up. Consecutive ejections may delay test results. Clinicians should stop using the affected cartridges and await manufacturer instructions.
Instrumentation Laboratory issued a high-severity recall for 1,126 GEM PAK cartridges used with the GEM Premier 5000. The recall cites increased PCSND errors during warm-up that can cause consecutive GEM PAK ejections. The issue may delay patient results. Hospitals should halt use and follow manufacturer instructions immediately.
ACME United Corporation is recalling Savannah Antibacterial Towelettes nationwide after CGMP deviations in manufacturing. The deviations may affect product quality and safety. Stop using the product immediately and contact ACME United or your healthcare provider for guidance.
Dynarex Obstetrical Towelettes Cleanser is under an active FDA recall as of Jan. 20, 2026. The recall cites CGMP Deviations that could affect product quality. Consumers and healthcare providers should stop using the product immediately and contact ACME United Corporation or a healthcare provider for guidance.