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. 2,653 recalls have been distributed to Washington in the last 12 months.
Showing 24901–24920 of 51,768 recalls
Recalled Item: NxStage PureFlow B Solution-RFP-404 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-406 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-403 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S & W White Beans Recalled by Faribault Foods, Inc. Due to Undeclared Sulfites
The Issue: Undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Tomato & Basil Hummus Dip Recalled by Bakkavor Foods USA, Inc....
The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Hummus quartet Recalled by Bakkavor Foods USA, Inc. Due to...
The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The PLEX Elite 9000 Recalled by Carl Zeiss Meditec, Inc. Due to Under...
The Issue: Under certain fault conditions, the existing design may expose the operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Septishield II Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Stopcocks Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...
The Issue: software malfunction; It was found when a user performs radiography using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.