1,120 recalls tagged with “electrical hazard”.
B BRAUN MEDICAL INC recalls 2,760 units nationwide due to a lid misalignment risk in the catheter connector. The recall covers the PERIFIX FX Continuous Epidural Anesthesia Tray and related components. Healthcare providers should halt use and follow manufacturer instructions for recall remedies.
HeartSine Technologies recalled 1,291,165 Pad-Pak defibrillator pads sold nationwide in the United States and worldwide. A defect may allow damage pins to disrupt the mechanical fit and electrical contact. Stop using the pads immediately and follow the manufacturer's recall instructions.
Taproom Gourmet bulk Empire Mix recall affects 3,547 cases distributed across New York, New Jersey, Connecticut, California, Illinois and Florida. The product lacks an ingredient label and contains undeclared allergens. Consumers should not consume the product and should seek a refund or replacement from Egress Capital Partners.
B Braun Medical has an active recall of the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide. The recall cites a potential mispositioned catheter connector lid. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
B Braun Medical recalled 10,130 ESPOCAN spinal/epidural trays nationwide after discovering potential for the catheter connector lid to be in an incorrect position. The recall covers multiple product codes and UDI numbers. Healthcare providers must stop using affected units and follow manufacturer instructions for remediation.
B BRAUN MEDICAL INC recalls 60 units of SESK Combined Spinal and Epidural Tray nationwide. The recall targets products distributed to all 50 states. The defective lid on the catheter connector may be in the incorrect position, posing a high-risk device issue. Stop using immediately and follow company instructions for recall remedies.
B Braun Medical recalled 2,840 NES1727KFX anesthesia tray kits distributed nationwide to healthcare facilities. The recall cites a potential mispositioned lid on the catheter connector. Healthcare providers should stop using the device immediately and follow recall instructions.
GE Medical Systems recalled 31 LOGIQ P10 R4.5 HD ultrasound systems sold nationwide in the United States and globally after discovering UGAP measurements may misstate liver steatosis. The UGAP data may display inaccurate values representing liver steatosis. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.
Percussionaire recalled 59,160 Phasitron 5 IPV In-Line Valve sets worldwide after an IFU update flagged a pressure-relief leak when used with ventilators. The defect endangers neonates and infants and patients under 10 kg with tidal volumes under 50 mL. Healthcare providers should halt use immediately.
Sprout Organics recalled 9,873 cases of 6+ Months Made With Organic Sweet Potato, Apple & Spinach baby food nationwide. A potential contamination with lead has been identified. Consumers who purchased the product should stop using it and contact Sprout Organics for refund or replacement through the recall notice.
Abiomed recalled 9,177 distributed Automated Impella Controllers worldwide over purge pressure concerns linked to purge retainer failures. The recall covers multiple product codes, including AIC w/Impella Connect for ECP (1000432) and various packaged controllers. Hospitals and clinicians should stop using the device and follow the manufacturer's recall instructions immediately.
FUJIFILM Healthcare Americas Corp recalled 16 CH-200 X-ray machines in the domestic market. The shaft that mounts the X-ray tube unit on the support may break. Protective parts may fail when the shaft breaks during frontward lifting. Healthcare providers should stop using the device immediately and follow recall instructions.
FDA recalls Carbamazepine Extended-Release Tablets, 400 mg, distributed nationwide by American Health Packaging. The recall cites failed dissolution specifications and class II classification. Consumers should stop using and contact healthcare providers for guidance.
GE HealthCare recalled 1 Optima NX dual-head gamma camera worldwide after detecting potential detector mounting failure if the unit is moved without proper support. The risk could cause a detector fall and life-threatening injury. Hospitals should stop using the device and follow the manufacturer’s recall instructions. Contact GE Medical Systems Israel Functional Imaging for guidance.
GE HealthCare Israel recalled 37 Maxicam dual-head gamma cameras distributed worldwide to hospitals. The recall cites potential detector mounting stress if the devices are moved without adequate support. This could result in a detector fall and life-threatening injury. Hospitals and healthcare providers should stop using the device and follow recall instructions from GE HealthCare.
UIH Technologies LLC is recalling 4 Shanghai United Imaging Healthcare uMI Panorama 35 MD PET/CT systems sold in the United States. A third-party outer cover can become trapped between the patient table and gantry during table movement. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions.
Philips North America recalls 28 Cardiac Workstation 5000 devices, model 860439, distributed nationwide in five states. A pinched power module wire led to a short during environmental stress tests. Users should stop using the device and follow manufacturer recall instructions.
Mars Foods US recalled 1,075 cases of Ben's Original Ready Rice Long Grain & Wild 8.8 oz sold in nine states. The hazard is the possible presence of stones in the product. Consumers should not consume the product and should contact Mars Foods US for refund or replacement by email.
GE HealthCare recalled 102 dual-head gamma cameras used for cardiac imaging worldwide after finding that some systems past the End of Guaranteed Service could be moved without adequate detector support. This could place excessive stress on detector mounting mechanisms and may cause a detector to fall, posing life-threatening risk. Hospitals and healthcare providers should stop using the devices IM
GE HealthCare is recalling 28 Elscint SPX6 dual-head gamma cameras worldwide. The recall cites detectors could be stressed during transport or relocation without adequate detector support, risking a detector fall and life-threatening injury. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.