325 recalls tagged with “electronic”.
Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition Taurine Mental & Athletic Performance dietary supplement distributed nationwide. The FDA enforcement report cites unapproved drug claims and misbranding. Consumers who purchased this product should not consume it and should contact the company for refund or replacement.
Glenmark Pharmaceuticals Inc., USA recalls 17,496 bottles of Carvedilol tablets sold nationwide after NNCI impurity exceeded FDA limits. The recall covers lot numbers 17241257, 17241258, and 17241279 with Exp. Date 06/2026. Consumers should stop using the product and contact Glenmark or their healthcare provider for guidance.
Wasatch Photonics recalled 192 Raman spectrometers in the United States after identifying two potential laser safety failure modes. Models 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC, and 785-ER-ILC are included. The defect could occur under excessive force or extreme continuous vibration. Stop using immediately and follow the manufacturer’s recall instructions.
Dynamic Sports Nutrition recalled 1,566 bottles of WINN-50 vanazolol dietary supplement sold nationwide. The FDA-listed recall cites degradation of an ingredient and sub-potent Vitamin B12. Consumers should stop using the product and contact the company for refunds or replacements.
Ortoma AB is recalling 261 Inserter Adapters for the Cup Inserter Tool used in hip replacement procedures sold worldwide, including Florida. The defect is weld breakage between the pin and the inserter holder. Surgeons and patients should stop using the devices immediately and follow the manufacturer's recall instructions.
Ford Motor Company recalls 2025 Expedition and other models over a brake booster software fault. The Electronic Brake Booster module may fail while driving or during ADAS use, reducing power brake assist. Ford will update the module software OTA or via dealer free of charge. Owner notifications started August 22, 2025. Contact Ford at 1-866-436-7332 for details and recall 25S77.
Curtis International Ltd. recalled Frigidaire-brand minifridges sold nationwide after more than $700,000 in property damage was reported. Internal electrical components can short circuit and ignite the surrounding plastic housing. Consumers should stop using recalled units immediately and contact Curtis for a full refund.
iMirror Inc. recalls Electric Bug Zapper Racket, Fly Swatter and Mosquito Swatter sold on Amazon and at imirror.com on July 24, 2025. The recall cites a hazard where the rechargeable battery can catch fire with extended use. Consumers should stop using the products immediately and contact iMirror for a full refund.
Pura Scents recalled the Pura 4 Smart Home Fragrance Diffusers sold at retailers on July 24, 2025. The detachable cover contains five magnets and can detach, creating an ingestion hazard for children. Consumers should stop using the diffuser immediately and contact Pura Scents for a free replacement front cover.
iStore recalled its Magnetic Wireless Power Bank, 5000 mAh, imported by Tomauri. The lithium-ion battery can overheat and ignite while charging. Only IST-09991/W05 units are affected; consumers should stop using the recalled power bank and return it for a full refund.
BioFire Defense recalled 130 FilmArray NGDS Warrior Panel NGDS-ASY-0007 kits distributed nationwide in the United States. The recall cites an increased risk of internal control failures when testing positive blood cultures. Clinicians should stop using the device immediately and follow recall instructions provided by BioFire Defense. Notification is by letter to affected facilities.
Boothwyn Pharmacy recalls 648 vials of semaglutide 2.5 mg/mL injection nationwide after detecting subpotent potency. The recall involves products distributed across the U.S. and is classified as Class II with a high hazard level. Stop using the product and contact Boothwyn Pharmacy or a healthcare provider for guidance.
Tandem Diabetes Care recalls 19 units of the t:slim X2 insulin pump with interoperable technology distributed internationally, including Israel. An app defect occurs when the phone uses a right-to-left language and can cause app-pump pairing problems and graphical defects. Patients should stop using the device immediately and follow the manufacturer’s recall instructions.
Ford Motor Company recalls certain 2025 Expedition and Navigator vehicles due to a passenger-side frontal air bag that may deploy with excessive force. Dealers will replace the passenger side air bags at no charge. Owner notification letters were mailed August 8, 2025.
bioMerieux recalled 235,269 VITEK 2 Gram-negative AST test cards containing Colistin cs02n, distributed internationally. The cards may produce false resistant results for Colistin when testing certain multi-drug-resistant bacteria. Healthcare providers should stop using the affected cards immediately and follow the recall instructions from bioMerieux.
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 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 1 mobile X-ray system in the United States. The device is distributed in CA, IL and NJ. The system is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have unspecified consequences. Clinicians and facilities should stop using the device and follow manufacturer instructions.
Sedecal recalled 6 mobile X-ray systems distributed in CA, IL and NJ after warning consignees the equipment is not water-resistant. Cleaning must follow the manual to avoid improper cleaning. Hospitals should stop using the devices immediately and follow recall instructions.
Sedecal SA recalled 6 SM-40HF-B-D-C mobile X-ray systems distributed to consignees in California, Illinois and New Jersey after a notice reminded users the devices are not water-resistant and must be cleaned strictly per the manual. The reminder outlined possible consequences of improper cleaning. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.