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. 2,496 recalls have been distributed to Oklahoma in the last 12 months.
Showing 21481–21500 of 28,654 recalls
Recalled Item: Wilson Penile Implantation System Retractor Frame Recalled by Abeon Medical...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Implant Cover Screw Dental implants Recalled by Biomet 3i, LLC Due...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical Healing Cap Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare PIIC Classic Upgrade Recalled by Philips Electronics...
The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Implant Straight Cover Screw Dental implants Recalled by Biomet 3i,...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...
The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locator Abutment Impression Coping Dental implants Recalled by Biomet 3i,...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain EP Twist Lock TM Coping Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...
The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prep-tite Cap Dental implants Recalled by Biomet 3i, LLC Due to Pouches may...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Twist Lock TM Coping Dental implants Recalled by Biomet 3i, LLC Due...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locator Replacement Housing Dental implants Recalled by Biomet 3i, LLC Due...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Cover Screw Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Twist Lock TM Coping Dental implants Recalled by Biomet 3i, LLC Due...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical EP Pick-Up Coping (Non-Hexed) Dental implants Recalled by Biomet 3i,...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System. Used to manage workflows for treatment...
The Issue: First Databank (FDB) is a third party product incorporated into MOSAIQ. FDB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Tower is the input device to program the Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...
The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.