1,046 recalls tagged with “electrical hazard”.
Bard Peripheral Vascular recalled 1,240 Safe-T-Centesis Catheter Drainage Trays due to safety indicator defects. The recall affects products distributed nationwide since November 6, 2025. The defect may cause serious injuries during use in medical procedures.
C.R. Bard Inc recalled 116 units of the InLay Optima Ureteral Stent Kit on November 6, 2025. The recall stems from a labeling discrepancy where the actual stent size may not match the product label. This recall affects distribution in multiple U.S. states and several countries worldwide.
Fresenius Kabi USA, LLC recalls 2,199,850 vials of Famotidine Injection, U.S. distribution nationwide plus Alaska, Hawaii and Puerto Rico after endotoxin testing concerns. The microbial contamination risk prompted an immediate stop-use order. Healthcare providers and patients should follow recall guidance and seek alternatives through their providers.
C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual stent size to differ from the labeled size. Healthcare providers and patients should stop using the device immediately.
The recall involves Neaude BR0221SL001 adult portable bed rails sold on Amazon. It poses a serious entrapment and asphyxiation risk. Consumers should stop using the recalled rails and start the refund process with Neaude now.
CareFusion 303 recalled 189 BD Alaris Pump Modules on November 6, 2025. The recall affects connectivity to hospital networks due to daylight savings time adjustments. Users should stop using the device immediately and follow manufacturer instructions.
Napei recalled its collapsible infant bath tubs sold on Amazon by Sefon Store after discovering the built-in thermometer uses button cell batteries that are accessible to children. The batteries pose a risk of ingestion, which can cause serious injuries or death. Stop using the tub immediately and contact Sefon Store for a free replacement battery compartment.
C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual size of the stent to differ from what is indicated on the label. The recall affects distribution across the U.S. and several countries worldwide.
Laiwu Manhing Vegetables Fruits Co recalled 245 cartons of irradiated onion granules sold in California after foreign objects were found in the powder. The contamination is described as black plastic planting film. Consumers should not consume the product and should contact the company for refund or replacement via email.
Datascope recalled 47 units of its Cardiosave Rescue Intra-Aortic Balloon Pump on November 4, 2025. The recall addresses a revised Preventative Maintenance schedule in the device's instructions for use. This issue poses a high risk to patient safety and requires immediate attention from healthcare providers.
Hyundai Motor America recalls 2025 Hyundai IONIQ 5 N vehicles with left-foot braking and N e-shift features. The recall cites potential reduced braking performance and continued acceleration after pedal release. Owners should avoid LFB and N e-shift until remedy is complete. OTA or dealer updates are free.
Datascope recalled 11,470 Intra-Aortic Balloon Pump systems on November 4, 2025. The recall addresses a revision in the Preventative Maintenance schedule as outlined in the Service Manual. Healthcare providers and patients must stop using these devices immediately.
GET TESTED INTERNATIONAL AB recalled 47 Blood Type Test units distributed nationwide in the United States after discovering the device was distributed without FDA premarket approval or clearance. The hazard is distribution without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and contact GET TESTED INTERNATIONAL AB for instructions.
GET TESTED INTERNATIONAL AB recalled 18 units of Neurotransmitters Plus on November 3, 2025. The recall occurred due to distribution without premarket approval or clearance. Patients should cease use immediately and follow manufacturer instructions.
Fresenius Kabi USA recalled 15,862 Ivenix Infusion Systems on November 3, 2025. The recall affects model LVP-0004 due to downstream occlusion alarms during low flow infusions. Healthcare providers and patients should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 10 units of the Pollen Allergy Test on November 3, 2025. The recall stems from distribution without necessary premarket approval. Patients should stop using the device immediately and follow manufacturer instructions.
GET TESTED INTERNATIONAL AB recalled 5 units of its Food Intolerance Test Small on November 3, 2025. The recall follows the distribution of the device without necessary premarket approval. Healthcare providers and patients must cease use immediately and follow the manufacturer's instructions.
GET TESTED INTERNATIONAL AB recalled 2 Gut Microbiome Test Mega units distributed nationwide in the United States. The recall centers on distribution without premarket approval or clearance. Consumers should stop using the device and contact the manufacturer for instructions. The notice was issued in 2025 and is currently active.
GET TESTED INTERNATIONAL AB's gonorrhea test was distributed nationwide in the United States. The recall cites distribution without FDA premarket approval or clearance. Patients and healthcare providers should stop using the test immediately and follow the manufacturer's recall instructions.
Fresenius Kabi USA recalls 483 LVP Primary Infusion Sets for the IVENIX infusion system nationwide in the United States. The recall cites incorrect assembly of a specific lot. Hospitals and clinicians should stop using the affected sets immediately and follow the manufacturer’s recall instructions.