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. 2,798 recalls have been distributed to Washington in the last 12 months.
Showing 7621–7640 of 29,208 recalls
Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...
The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #:...
The Issue: Assigned vial lot numbers for the incorrect type of product. SARS-CoV-2 &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C6 Recalled by Hamilton Medical AG Due to Due to a malfunction...
The Issue: Due to a malfunction related to the backlight on the ventilator screen. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...
The Issue: Due to increase in Li-Ion Battery failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...
The Issue: Detachment controller, of an aneurysm embolization system, has an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simple Clamp Recalled by Baxter Healthcare Corporation Due to the adhesive,...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Standard Starburst Recalled by Baxter Healthcare Corporation Due to...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Advance Table Recalled by Baxter Healthcare Corporation Due to the...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Life Assist Beach Chair Recalled by Baxter Healthcare Corporation Due...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Polar Head Positnr-Device Only Recalled by Baxter Healthcare...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beach Chair Clamp Recalled by Baxter Healthcare Corporation Due to the...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X (IS4200) and Xi (IS4000) systems Recalled by Intuitive Surgical,...
The Issue: Inadvertent energy delivery from surgical system instrument if 1) Force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium (Li) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.