1,046 recalls tagged with “electrical hazard”.
SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.
Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.
Wegmans Food Markets is recalling 521 units of Wegmans Large Ultimate Plain Cheesecake sold in Virginia, Maryland, North Carolina and Washington D.C. The product contains undeclared pecans. Consumers should stop using the product and contact Wegmans for refund or replacement.
Synthes (USA) Products LLC recalled 120 low-profile locking screws for intramedullary nails used in the RFN-Advanced Retrograde Femoral Nailing System and the Tibial Nail Advanced System. The recall covers devices distributed worldwide through healthcare providers. The external packaging mislabels screw lengths: 42 mm screws are labeled 46 mm and 46 mm screws are labeled 42 mm. Hospitals and spine
Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.
Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Tray with Strawberries after potential Listeria monocytogenes contamination. The recall covers trays packed in Minneapolis, MN and distributed to Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The product should not be consumed and refunds or replacements are being offered. The recall is active as of the latest notice.
Sunbeam Products recalled more than 1 million Oster French Door Countertop Ovens after reports of doors closing unexpectedly and causing burn risks. The recall covers four Oster models and affects units sold nationwide. Consumers should stop using the ovens and contact Sunbeam for a free repair kit.
Aloe Up recalled 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 sold nationwide in the United States. The recall cites cGMP deviations after the product failed total aerobic microbial count testing. Consumers should stop using the product and follow guidance from SV Labs Prescott Corporation or a healthcare provider.
Volkswagen Group of America recalls one 2025 Audi SQ7 over a potential fuel leak from an improperly tightened high pressure fuel pump. The recall affects a single vehicle and is classified as high risk due to fire potential. Owners should contact Volkswagen for inspection and repair at no cost.
Audi and Volkswagen Group of America recall 2025 GTI, Golf R, Audi A5, A6 Sportback E-Tron, S5, S6 Sportback E-Tron, 2026 Q4 Sportback E-Tron and Q4 E-Tron vehicles. The torsion bar in the front seat belt retractors may be damaged during production. Dealers will replace one or both front seat belts at no charge. VIN lookups begin Sept 26, 2025 and owner letters go out Nov 21, 2025.
Zydus Lifesciences and Zydus Pharmaceuticals USA recall 600 bottles of Entacavir 1 mg tablets distributed nationwide in the United States. An out-of-specification organic impurity triggered the recall. Stop use immediately and contact a healthcare provider or Zydus for guidance.
BD recalled 2,050 units of the EpiCenter Microbiology Data Management System due to unauthorized access to product service credentials. The defect could allow access to confidential data. Stop using affected devices and follow manufacturer guidance for updates or replacement.
Beckman Coulter recalls 160 DxC 500i Clinical Analyzer Modules and the DxI 9000 Access Immunoassay Analyzer worldwide after a software anomaly could misapply manual dilution factors. The defect affects samples already in progress using the same Sample ID. Stop using the devices immediately and follow the recall instructions. Beckman Coulter will provide instructions via the recall process.
Kico Knee Innovation recalls 21 ARVIS Shoulder systems nationwide after reports that AI planning software may cause implant malalignment or reduced range of motion. The recall covers software version V2025.1.2 used with IN-27300 hardware. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
IcyBreeze recalled the IcyBreeze Buddy portable misting fan due to a charging fire hazard. The recall affects consumers who own the IcyBreeze Buddy with a 1.5-liter water tank and a 10,000 mAh lithium-ion battery. Affected units must be returned for a full refund and disposal guidance. Call 817-900-2664 or visit the recall page to begin the process and receive a $150 credit at Solo Brands brands.
Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.
LXDHSTRA recalled baby loungers and crib bumpers on September 18, 2025. The recall covers LXDHSTRA-branded loungers sold online at Amazon. The defect involves suffocation and fall hazards linked to design and ban violations. Stop using immediately and seek a full refund from LXDHSTRA.
YooxArmor recalled its multi-purpose kids’ helmets sold on Amazon after safety violations. The helmets fail to meet the mandatory bicycle helmet standard for impact attenuation, stability, labeling and certification. Consumers should stop using the helmets and request a full refund from YooxArmor.