1,120 recalls tagged with “electrical hazard”.
Ford Motor Company recalls 2025 F-250 SD and other SD models for a brake pedal pushrod retaining spring that may not be installed. The defect can cause a sudden loss of brake function and a crash risk. Owners should not drive the vehicle until repaired. Ford will inspect and repair the brake pedal assembly free of charge; letters were mailed June 20, 2025.
VANTIVE US HEALTHCARE recalled 13,760 Prismaflex TPE2000 Sets on January 6, 2026, due to a potential dislodgement hazard. The recall affects the deaeration chamber of the Prismaflex Control Unit. Healthcare providers and patients must stop using the device immediately.
VANTIVE US Healthcare recalled 230,596 units of the PRIMSAFLEX M100 Set on January 6, 2026. The recall follows a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.
VANTIVE US Healthcare recalled 137,576 Prismaflex M150 Sets on January 6, 2026. The recall addresses a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Encore Medical, LP recalled 19 units of the EMPOWR 3D Knee Tibial Insert on January 5, 2026. The recall follows the discovery of a packaging error that may cause surgical delays. Healthcare providers and patients should stop using the device immediately.
Raz Design Inc recalled 66 Raz Mobile Shower Commode Chairs nationwide, citing a modification that may allow the seat to detach if outside rear brackets are not properly engaged. The recall covers multiple catalog numbers and serial ranges. Patients and healthcare providers should stop using the device immediately and contact Raz Design for instructions.
Alphatec Spine recalled 7 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The incorrect navigated array connection geometry poses a high hazard risk in surgical settings. Healthcare providers and patients must stop using the devices immediately.
Alphatec Spine recalled 15 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The navigated array connection geometry is incorrect, posing risks during surgical procedures. Healthcare providers and patients should stop using the instruments immediately.
AVID Medical recalled 1,500 units of the TRANSPORT BAG KIT on January 2, 2026. A seal issue with the Tyvek bag may compromise the sterility of the kit. The recall affects healthcare providers and patients in New Jersey.
Kia America recalled 2025 Sorento Hybrid and 2024-2025 Sorento SUVs sold at Kia dealerships nationwide after a body domain control software fault may disable low beam headlights and taillights. The defect can reduce visibility and raise crash risk. Owners should contact a Kia dealer for a free software update under recall SC331; notifications were mailed Feb. 21, 2025.
Centinel Spine recalled 20 units of the Prodisc C SK cervical disc on December 31, 2025. The products were mislabeled as the 6mm variant but included the 5mm variant. The recall affects patients in multiple states including California and New York.
Medline Industries recalled over 926,000 IV Administration and Extension Sets due to a significant risk of leaks and breaks. The recall affects multiple models with potential exposure to chemicals and mechanical forces. Users should discontinue use immediately to prevent serious health risks including blood loss and infections.
Miach Orthopaedics recalled 284 units of the BEAR Implant, Model Number 1000, on December 31, 2025. The recall stems from an incorrect expiration date on the label that exceeds the product's approved shelf life. Patients and healthcare providers should stop using the device immediately and follow recall instructions.
Intuitive Surgical recalled 47 da Vinci 5 Surgeon Console Viewer Displays on December 30, 2025. The devices may lose display functionality, risking surgical injury. Healthcare providers should stop using the consoles immediately and follow recall instructions.
Siemens Medical Solutions USA recalled five LUMINOS Q.namix T X-ray systems on December 29, 2025. The recall affects devices that can process images from previous patients due to a software issue. Healthcare providers must stop using these devices immediately.
Siemens Medical Solutions USA recalled 40 units of its LUMINOS Q.namix R X-ray system on December 29, 2025. The recall addresses a defect that may result in images being incorrectly processed, potentially showing images from previous patients. Healthcare providers should stop using the device immediately and follow recall instructions.
Medline Industries, LP recalled 4,300 blood culture kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with packaging that may exhibit an open seal. This defect poses a high risk to patient safety.
Zimmer Surgical Inc recalled 206 A.T.S. 5000TS Tourniquet Systems on December 24, 2025. The device can freeze or become unresponsive in certain non-English language settings. This issue may delay patient care during emergencies.
GE Healthcare recalled 364 Omni Legend systems on December 24, 2025, after reports of image quality issues. The recall affects multiple models distributed worldwide, including the Omni Legend 16 and 21. Users should stop using the devices immediately due to potential diagnostic inaccuracies.
Medline Industries, LP recalled 1,350 medical convenience kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potential open seals. Users should cease using these kits immediately and follow manufacturer instructions for return.