239 recalls tagged with “repair available”.
Babyletto recalled its Kiwi Electronic Recliner and Glider chairs due to an overheating USB module. The USB module can overheat and spark, posing an overheating hazard. Consumers should stop using the recalled chairs and contact Babyletto for a free repair kit.
Giant Bicycle recalls Momentum Vida E+ electric bicycles after a fork crash hazard. The recall affects bikes with specific serial numbers. Stop riding and contact Giant Bicycle for a fork replacement.
Boothwyn Pharmacy recalls 8 vials of Fluorescein 2% Ophth 3 mL nationwide after a subpotent drug finding. The recall was issued July 9, 2025 and remains active.
Honda recalls 2025 CR-V Hybrid vehicles sold through Honda dealers nationwide after finding an improperly installed fuel feed hose that may leak. The recall is identified by Honda as TLS. Dealers will replace the fuel feed hose and install a new connector cover at no charge. Owners should contact Honda at 1-888-234-2138 for service.
Volkswagen Group of America recalls 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 models for loose bolts in the chassis, brake system and suspension. The potential consequence is loss of vehicle control and a crash risk. Owners should stop driving the vehicle and contact a dealer for inspection; recall letters were mailed on July 25, 2025.
Orthofix U.S. recalled 3 Pillar SA Ti intervertebral body fusion devices nationwide in the United States after a labeling discrepancy. The 37 mm implant width is correct on the front label, but the outer side flap and inner label information box incorrectly state 33 mm. Healthcare providers and patients should stop using the device immediately and await manufacturer instructions.
Sedecal SA recalled 14 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey after notifying consignees by email that the devices are not water-resistant. The company says cleaning must follow the manual strictly, warning about possible consequences of improper cleaning. Healthcare facilities and patients should stop using the devices immediately and follow the REMS
Sedecal recalled 2 units of the SM-40HF-B-D-C 40KW 55G/60G Mobile X-ray system after warning consignees that the device is not water-resistant and must be cleaned exactly according to the manual. The notice outlines the potential consequences of improper cleaning. Healthcare facilities in California, Illinois and New Jersey should stop using the device immediately and contact Sedecal for further 1
Sedecal SA recalls 56 mobile digital diagnostic X-ray systems distributed to facilities in California, Illinois and New Jersey. An email reminds users the equipment is not water-resistant and must be cleaned exactly as the manual prescribes. Stop using the device and follow the recall instructions.
Sedecal SA recalled 22 SM-32HF-Batt 32KW analog mobile X-ray systems distributed to California, Illinois and New Jersey. The units are not water-resistant and must be cleaned strictly per the manual, with explicit consequences for improper cleaning. Healthcare facilities should stop using the devices immediately and follow the manufacturer's recall instructions sent by email.
Sedecal recalled 1,198 MobileDiagnost wDR 2.2 mobile X-ray systems distributed in California, Illinois and New Jersey. The company reminded users the equipment is not water-resistant and must be cleaned strictly according to the manual. Improper cleaning could have consequences outlined by Sedecal. Health care providers should stop using the device immediately and follow recall instructions.
Sedecal recalled 8 units of the Easy Moving Plus mobile X-ray system distributed in California, Illinois and New Jersey. The devices are not water-resistant and cleaning must follow the manual to avoid the consequences of improper cleaning. Stop using the device and contact Sedecal SA or your healthcare provider for instructions.
Mercedes-Benz USA is recalling certain 2024 GLE 350 4MATIC, 2025 GLE 450e 4MATIC, and additional models sold through its dealer network. The issue involves a multi-purpose camera and rearview mirror that may detach from the windshield. Dealers will replace the windshield and reinstall the camera and mirror at no charge.
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.
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.
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.
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
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.
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.