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. 2,469 recalls have been distributed to Washington in the last 12 months.
Showing 45101–45120 of 51,768 recalls
Recalled Item: Liquid Mouse Monoclonal Antibody CD15 (NCL-L-CD15) Recalled by Leica...
The Issue: Product does not function as intended up to the expiry date on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T:slim Insulin Delivery System Insulin Infusion Pump Recalled by Tandem...
The Issue: Specific lots of insulin cartridges that are used with the T:slim Insulin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct assay Recalled by Focus Diagnostics Inc Due to...
The Issue: Focus Diagnostics is initiating an urgent safety notice correction for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aminosyn 3.5% M Sulfite-Free Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products White Slides Recalled by Ortho-Clinical...
The Issue: An incorrect assay value (0.3785) was printed on the product carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-AB Abdominal Dressing Kit with Soft Port Recalled by...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS Soft Port (The RENASYS Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-G Sterile Recalled by Smith & Nephew Inc. Due to...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933 Recalled...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F XL with Soft Port REF #: Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System is an implant system designed...
The Issue: The product may be mislabeled and could result in the incorrect implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Recalled...
The Issue: Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...
The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panaroma Central Station Product Usage: This device can view real time...
The Issue: Mindray has identified two issues with the Panorama Central Station. Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS...
The Issue: Janssen Diagnostics, LLC received complaints of camera failures on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFSITE¿ Injection Sites and IV Sets manufactured with SAFSITE¿ Injection...
The Issue: Complaints were received reporting leakage on certain lots of SAFSITE¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Template and the Saw Guide for the Ulna Osteotomy Recalled by Synthes,...
The Issue: The Drill Template and the Saw Guide for the Ulna Osteotomy System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Driving Cap/Threaded Both parts are intended for use in Recalled by...
The Issue: The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.