2,229 recalls tagged with “stop use immediately”.
PRIMO No. 1 in Produce recalled 89 boxes of peeled/diced cucumbers distributed to VA, NY, PA and NJ after Salmonella contamination was detected. The recall is Class I with a HIGH hazard level. Do not consume the cucumbers and contact PRIMO No. 1 in Produce for a refund or replacement.
PRIMO NO. 1 IN PRODUCE recalled 89 boxes of peeled-sliced cucumbers distributed to Virginia, New York, Pennsylvania and New Jersey after Salmonella contamination was detected. The recall was issued on May 20, 2025. Consumers should not eat the product and should contact PRIMO NO. 1 IN PRODUCE, INC for refund or replacement.
Chefs Warehouse recalled 15 lbs of diced cucumbers distributed to Maryland, Delaware and Virginia after Salmonella contamination was found. The recall is active as of May 20, 2025. Consumers should not consume the product and should contact Chefs Warehouse for refund or replacement.
Chefs Warehouse recalled 190 cases of Cucumber Select 15ct sold through Chefs Warehouse after Salmonella contamination was detected. The recall is a Class I action and carries a high hazard. The recalled lots were distributed to Maryland, Delaware and Virginia; the recall was issued May 20, 2025.
Chefs Warehouse recalled 98 cases of cucumber distributed to Maryland, Delaware and Virginia after Salmonella contamination was detected. The product is contaminated with Salmonella. Consumers who bought this cucumber should not consume it and should contact Chefs Warehouse for a refund or replacement.
Medtronic MiniMed recalled 1,440 Simplera Sensor units distributed outside the United States after a device cap label may not adhere, risking sterility. The defect could increase infection risk. Patients and healthcare providers should stop using the device and follow recall instructions provided by Medtronic MiniMed or their healthcare provider.
Turkana Food Inc. recalled 352 cases of Floria Dried Apricots, 200-gram packages, distributed to retailers in 19 states. The recall was issued on April 29, 2025. The product contains undeclared sulfites. Consumers should not eat it and should contact Turkana Food Inc. for refund or replacement via email.
3M recalled 530,470 Ranger Blood/Fluid Warming High Flow Sets due to incorrect flow rates and outlet temperature locations. This defect can affect the warming of fluids, posing serious risks to patients. Healthcare providers must stop using these devices immediately and follow the manufacturer’s instructions for returns.
Ford recalls 2024-2025 F-150 and Expedition and 2024 Navigator SUVs due to a misaligned engine cup plug that can cause a rapid oil leak. The leak may stall the engine and, if oil contacts hot parts, can ignite a fire. Ford says dealers will inspect and replace the plug at no charge; owner letters were mailed May 22, 2025.
Honda recalled 2024-2025 ADV160 scooters after discovering the oil pump driven gear may fail, causing a loss of drive power. The loss of drive power could lead to a crash. Owner letters were mailed August 6, 2025, and dealers will replace the gear free of charge under recall KR9.
Chrysler recalls 2025 Jeep Wagoneer S BEVs after headlight aim adjustments fail to meet FMVSS 108. Dealers will correct by adjusting plugs at no charge. Letters to owners began April 3, 2025. No injuries reported in the notice.
AUDI Q4 E-Tron and ID.4 models are recalled by Volkswagen Group of America for a faulty on-board charger that may stop charging the 12-volt system. The recall affects 2024-2025 models. Dealers will replace the on-board charger free of charge. Letters notifying owners were mailed May 20, 2025.
BMW recalls 2025 X3 30 xDrive vehicles due to an overheated positive battery cable connection that can cause engine stall and fire risk. The recall affects 2025 X3 models and affects owners nationwide. Dealers will inspect and tighten or replace the positive battery cable and starter-generator at no charge. Letters to owners were mailed June 5, 2025.
World Perfumes Inc. recalled 3,900 bottles of Iodo Blanco Iodides First Aid Antiseptic in Florida after broken or leaking containers were reported. The recall covers iodine 2% antiseptic distributed by Essential Products. Consumers should stop use immediately and contact World Perfumes or a healthcare provider for guidance.
Honda recalled 2025 Pilot SUVs and related Acura MDX Type-S and TLX Type-S vehicles sold through Honda and Acura dealer networks after a FI-ECU software error may cause engine stall or a loss of power. Dealers will reprogram the FI-ECU at no charge. Owner letters were mailed March 17, 2025. Contact Honda customer service at 1-888-234-2138 for recall EL1 and AL0. For updates, use the NHTSA hotline
Subaru of America, Inc. is recalling certain 2025 Forester vehicles equipped with 18-inch aluminum alloy wheels. The lug seat surface may be incorrectly specified, which can cause the wheel to detach and reduce vehicle stability. Owner notification letters were mailed February 28, 2025, and dealers will inspect and replace the wheels as necessary at no charge.
CorNeat Vision recalled EverPatch surgical matrix (REF 1036295) in a worldwide distribution that includes 50 states and several countries. The recall addresses retroactive labeling corrections to include prevention and management of would dehiscence. Healthcare providers and patients should stop using the device and follow the manufacturer's recall instructions.
Olympus Corporation of the Americas recalled 633 units of the Cystoscope Outer Sheath, Model WA22810A on September 13, 2024. The recall occurred due to potential device damage when used with a GreenLight Laser for BPH therapy. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Omnia Medical issued a recall for 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device and TiBrid SA Angled Screwdrivers after field failures were reported. The recall covers nationwide distribution in AZ, CA, NJ, NV, OK and WA. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.
Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device SA Angled Punch Awl. The recall covers models 17-5A-AWL3, 17-5A-AWL4, 17-5A-AWL5 with UDI 00843511113056 and 00843511122287/22294. The hazard is failure of fusion system instruments in the field. Consumers should stop use and follow recall instructions.