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. 2,007 recalls have been distributed to Washington in the last 12 months.
Showing 15381–15400 of 29,208 recalls
Recalled Item: IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1 Recalled by CMP...
The Issue: Foreign material in product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A Recalled by Baxter...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA Bags - 3000 mL Product Usage: A Recalled by Baxter...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA Bags - 1000 mL Product Usage: A Recalled by Baxter...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA Bags - 2000 mL Product Usage: A Recalled by Baxter...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Technoflux IMPAK Resina lfquida acrilica elastic Curado-Calor Tipo 1...
The Issue: Foreign material in product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA Bags - 500 mL - Product Usage: Recalled by Baxter...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium TL Steerable Inserter Recalled by Howmedica Osteonics Corp. Due to...
The Issue: The firm received complaints related to the locking mechanism on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiLite X-Short anti-tip tubes Recalled by TiSport, Llc Due to The anti-tip...
The Issue: The anti-tip tubes potentially fail in certain situations and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROCARE B20 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...
The Issue: Patient monitors may restart due to network overload caused by network...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B20i Patient Monitor and B20i V2 Patient Monitor. The device Recalled by GE...
The Issue: Patient monitors may restart due to network overload caused by network...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B40i Patient Monitor and B40i Patient Monitor V3 The device Recalled by GE...
The Issue: Patient monitors may restart due to network overload caused by network...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROCARE B40 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...
The Issue: Patient monitors may restart due to network overload caused by network...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B105/125 Patient Monitor. The device is a portable multiparameter unit...
The Issue: Patient monitors may restart due to network overload caused by network...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...
The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME)...
The Issue: Firm identified an issue in the manufacturing process which might contribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...
The Issue: Potential for outer pouch sterile barrier to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...
The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...
The Issue: The action is being initiated because the cooling indicator board was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APS Accelerator modular systems Recalled by Abbott Laboratories, Inc Due to...
The Issue: The firm identified customer sites where modules which the safety pacemaker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.