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. 1,183 recalls have been distributed to Washington in the last 12 months.
Showing 1321–1340 of 51,768 recalls
Recalled Item: HeartSine Pad-Pak Recalled by HeartSine Technologies Ltd Due to Due to...
The Issue: Due to customer complaints, defibrillator pads may contain damage pins that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combined Spinal and Epidural Anesthesia Tray 2 Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL INC...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Recalled...
The Issue: Software issue for hq analyzer results in system not visibly applying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenith Alpha 2 Thoracic Endovascular Graft Recalled by Cook Medical...
The Issue: Affected devices may contain PTFE coating scrapings. Scrapings could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Recalled by Fisher & Paykel Healthcare, Ltd. Due to When...
The Issue: When unintentionally disconnected from power source, humidifier device (used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESPOCAN Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7....
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7....
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Recalled...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P10 series with software version R4.5.7 Model Number 5877534 Recalled...
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure Recalled...
The Issue: InSure ONE failed sensitivity testing when used with Test Card Lot T241102,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Software Builds 3.1.3 Recalled by ELEKTA...
The Issue: When appending a care plan that contains one or more wave medication orders,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haifa COLD SMOKED SEABASS 8 OZ Recalled by D & M Smoked Fish, Inc. Due to...
The Issue: Contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.