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. 2,840 recalls have been distributed to Washington in the last 12 months.
Showing 1101–1120 of 51,768 recalls
Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...
The Issue: The heat function may become damaged over time due to patients pressing on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...
The Issue: The heat function may become damaged over time due to patients pressing on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone)...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ Controller (standalone)...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Recalled...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk5000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UUltrasound System 2300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1202 Flex Focus Ultrasound System Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3500 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Max Fusion XXX Recalled by Mohamed Hagar Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sprouts Smoked Mozzarella Pasta Salad Recalled by Sprouts Farmers Market Due...
The Issue: Product may contain Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fasenra (benralizumab) Injection Recalled by ASTRAZENECA PHARMACEUTICALS Due...
The Issue: Lack of Assurance of Sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...
The Issue: Automated cell-locating device barcode reader may read the barcode of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...
The Issue: The device may either fail to start up, or the transducer may start briefly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...
The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...
The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...
The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.