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. 2,719 recalls have been distributed to Washington in the last 12 months.
Showing 20281–20300 of 51,768 recalls
Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software bug may lead to one image to be assigned to two different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dutasteride Capsules Recalled by AVKARE Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Garbanzo Beans Recalled by Attilio A Merlino and Associates Inc Due to...
The Issue: Product is recalled due to the potential presence of glyphosate.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...
The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THP Hip Plating System Recalled by Zimmer Biomet, Inc. Due to Potential...
The Issue: Potential increase in fracture rate was detected during internal testing, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dry Garbanzo Beans are sold under different brands and described Recalled by...
The Issue: 11.8 ppm of glyphosate was detected in dry garbanzo beans.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The 13 Bean Soup Mix product is distributed in 2000 Recalled by Columbia...
The Issue: Product was recalled due to a potential for contamination with glyphosate.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...
The Issue: When inflating/deflating a single bladder, both bladders could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...
The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.