Product Recalls in Washington
Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,814 recalls have been distributed to Washington in the last 12 months.
Showing 6061–6080 of 29,208 recalls
Recalled Item: Cios Select VA 21 with FD- A Mobile X-ray system Recalled by Siemens Medical...
The Issue: Incorrect glue was applied on the plexiglass sheet on the single tank cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options¿ / Epidural anesthesia kit (10 count carton) Recalled by B....
The Issue: Kits were assembled with the incorrect Filter Straw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Clostridium difficile Nucleic Acid Test Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Enteric Pathogens Nucleic Acid Test (EP) Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix¿ / Epidural anesthesia kit (10 count carton) Recalled by B. Braun...
The Issue: Kits were assembled with the incorrect Filter Straw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...
The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Shots were...
The Issue: Shots were terminated by the mAs integrator; however, the 4 ms exposure time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trexo Device Recalled by Trexo Robotics Holdings Inc. Due to Electrical...
The Issue: Electrical issues that could potentially render the device non-functional,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UFSK Treatment chair 500 XLE- Treatment chair for positioning and Recalled...
The Issue: Service life of the electrical seat part drive of the treatment chair may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.