1,030 recalls tagged with “electrical hazard”.
DermaSensor recalled 343 diagnostic devices on October 13, 2025, due to a risk of incorrect results. The recall affects nine units specifically identified for failing to meet specifications. This issue could delay patient referrals for necessary treatment.
MRIMed recalled 314 batteries for the SL-110 Mobile Exam Light on October 13, 2025. The batteries can overheat while charging, melting internal components and producing smoke. This recall affects devices distributed in the U.S. and several countries worldwide.
Mylan Institutional LLC recalled 800 vials of Haloperidol Lactate Injection on October 10, 2025, due to incorrect RFID tag labels. The product may pose a risk due to potential mislabeling affecting tracking and administration. Healthcare providers should stop using the product immediately and follow up with Safecor Health for guidance.
Thoratec recalled 8,399 CentriMag Blood Pumps on October 10, 2025, due to a significant malfunction risk. The blood pump may not securely lock into the motor, potentially leading to serious health complications. The recall affects models distributed worldwide, including across the United States and several countries.
Glycar SA Pty. recalled 18 units of the SJM Pericardial Patch on October 9, 2025. The affected lot may not meet required tensile strength specifications. Healthcare providers and patients should stop using this device immediately.
Pivotal Health Solutions recalled 34 heated massage tables on October 9, 2025. The heat function may overheat, posing a risk of smoldering and melting. Affected units are distributed nationwide in the U.S., Canada, and Japan.
EcoFlow Technology recalled Delta Max 2000 Power Stations due to a fire hazard. The recall affects model EFD310, identified by a black and silver design. Consumers should stop using the product immediately and seek a firmware update for repair.
C-RAD POSITIONING AB recalled 189 Catalyst and Catalyst+ devices on October 9, 2025, due to issues with stereotactic radiosurgery (SRS) treatment. The defect may lead to incorrect patient positioning, potentially compromising treatment effectiveness. The recall affects devices distributed across 37 countries, including the United States.
Volkswagen recalled certain 2025 ID. Buzz vehicles on October 4, 2025. The brake system warning light may display incorrect symbols and colors. This defect increases the risk of a crash.
ICU Medical recalled 23,203 IV administration sets on October 2, 2025. The sets lack an internal shutoff valve, risking fluid over-delivery and air infusion. This recall affects devices distributed worldwide, including the U.S., Canada, Australia, and New Zealand.
Abiomed issued a recall for 10,153 Automated Impella Controllers on October 1, 2025. The devices face potential cybersecurity vulnerabilities related to their operating system. Healthcare providers and patients should stop using these devices immediately.
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.
B BRAUN MEDICAL recalled 1,298,454 hemodialysis bloodlines on September 30, 2025. The recall results from the risk of micro-air bubbles due to damaged connectors. Patients should stop using the product immediately and follow the manufacturer’s instructions.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 x-ray systems on September 29, 2025. The devices may suffer from corrosion of the Image Intensifier Television control board, leading to poor image quality. Users must stop using the device immediately and follow the recall instructions.
Synthes (USA) Products LLC recalled 120 units of medical screws on September 26, 2025. The screws were incorrectly labeled, posing a risk to patients. The recall affects multiple states and Canada.
Synthes (USA) Products LLC recalled 122 surgical screws on September 26, 2025. Mislabeling of screw lengths poses a serious risk to patients. Affected products include those used in the RFN-ADVANCED and Tibial Nail Advanced Systems.
LeMaitre Vascular recalled one unit of its Collagen Vascular Graft on September 25, 2025. The device was packed in the wrong size labeled outer packaging, posing a high hazard to patients. Health providers and patients should stop using this device immediately and follow the recall instructions.
Becton Dickinson & Co. recalled 177 units of the BD BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a high risk to patient data and device integrity. Healthcare providers must stop using the devices immediately and follow recall instructions.
Becton Dickinson & Co. recalled 1,086 units of its BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a risk to data security. Affected systems include the BACTEC 9120 with catalog numbers 445570 and 445702.
Biomet recalled 98 units of its ZipTight Acute AC Joint Implant on September 23, 2025. The recall follows reports of a potential missing slotted button assembly in one lot. Patients and healthcare providers must stop using the device immediately.