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. 1,923 recalls have been distributed to Washington in the last 12 months.
Showing 26741–26760 of 29,208 recalls
Recalled Item: Brand Name: SV Elastomeric Infusion Device. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Multirate Infusor Devices. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201101 Femur CR POROUS FEM COMP SIZE AML Rx Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597106126 Provisional ALL POLY PAT PROV MICRO SZ 26 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00587806126 Patella MICRO POROUS PAT 26MM X 10MM Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595201201 Femur CR-FLEX POR FEM B-L Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595001201 Femur CR-FLEX PCT FEM B-L Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201333 Femur CR POR SURF HDN FEM CO-NID CML Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90595202017 Articular Surface XLPE CR ART SURF AE12/PUR 17 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001303 Femur CR PRC FEM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597206126 Patella ALL POLY PAT COMP MICRO 26DIA Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201303 Femur CR POR FM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597101101 Provisional CR PROV FRM COMP SIZE AML Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.