Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 26201–26220 of 28,654 recalls
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: 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: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Medtronic recently identified an issue with a subset of Consulta¿ CRT-P and...
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: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: Infusor SV and LV Elastomeric Infusion Devices. Indicated...
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: Multiday lnfusor Recalled by Baxter Healthcare Corp. Due to Due...
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 10 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: Brand Name: Basal/Bolus Infusor. 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: 00597201131 Femur CR POR SURF HDN FEM CO-NID 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: 00598706201 Provisional CRA FEM PROV/CUT GDE SZ BML 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: 00597102010 Provisional CR ART SURF PROV 12/PURPLE 10 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: 00597502010 Provisional AC ART SURF PROV 12/PUR 10 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: 00597602010 Articular Surface AC ART SURF 12/PUR 10 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: 00597601201 Femur CRA PRECOAT FEM COMP SIZE B/L 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: 00597202009 Articular Surface CR ART SURF 12/PURPLE 09 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: 00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9 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: 00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10 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.