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. 2,794 recalls have been distributed to Washington in the last 12 months.
Showing 10241–10260 of 29,208 recalls
Recalled Item: Synapse PACS - Radiological Image Processing System - Product Usage:...
The Issue: The wrong patient information may be displayed in the viewer or PowerJacket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to...
The Issue: Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cellex qSARS-Cov-2 Antigen Rapid Test Recalled by Cellex Due to The kit does...
The Issue: The kit does not have an emergency use authorization (EUA).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyWay Walker Chassis - Product Usage: is intended for use Recalled by James...
The Issue: Due to a failure of the welds, the casters detached from the rear legs of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic pulsed doppler imaging system - Product Usage: intended for...
The Issue: Arietta 850 software version 4.0.0., 4.0.1, and 4.0.2 has an error in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe HVAD Controller Connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe Expected Alarm Duration. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...
The Issue: Their is a potential that Video Processor/Illuminators may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to There is a...
The Issue: There is a potential for tube trays to leak which could potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF Delivery Dev Caps Bravo x5 Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System - Product Usage: developed for...
The Issue: Siemens has become aware of a potential issue in which the imaging system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE DIAGNOSTICS FenomPro SN ***** - Product Usage: a portable Recalled by...
The Issue: Erroneously high FeNO levels which may contribute to premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Treatment Delivery System - Product Usage: indicated for...
The Issue: The set screws that connect the Standard Treatment Couch linkage arm to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit - Product Usage: intended for use in Recalled by Fenwal...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus MNC Apheresis Kit - Double Needle - Product Usage: Recalled by Fenwal...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Infusion Pump 8100 Bezel (plastic piece only) Recalled by Tenacore...
The Issue: Bezel repair parts used, not by the original manufacturer, to service and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit Therapeutics - Product Usage: intended for use Recalled...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Infusion Pump Module Recalled by Tenacore LLC Due to Bezel repair...
The Issue: Bezel repair parts used, not by the original manufacturer, to service and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.