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. 2,654 recalls have been distributed to Oklahoma in the last 12 months.
Showing 5541–5560 of 49,976 recalls
Recalled Item: Abbott Proclaim Plus 7 Implantable Pulse Generator Recalled by Abbott...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim DRG Implantable Pulse Generator Recalled by Abbott Medical...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 7 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Liberta RC Recalled by Abbott Medical Due to Deep brain stimulation...
The Issue: Deep brain stimulation system will first turn off after approximately 50...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 3028 Recalled by Inspire Medical Systems Inc. Due to There is...
The Issue: There is a potential manufacturing defect which can lead to electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of Recalled by...
The Issue: Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper FD10 system with an ADN7NT patient table. Recalled by...
The Issue: When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper FD20 Biplane system with an ADN7NT patient Recalled by...
The Issue: When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper FD20 system with an ADN7NT patient table. Recalled by...
The Issue: When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EYLEA Recalled by Regeneron Pharmaceuticals Inc Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Complaints of syringe breakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A610 Clinician Programmer (CP) Software Application (app) with the following...
The Issue: Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UPPER EXTREMITY PK Recalled by American Contract Systems Inc Due to Ethylene...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL KNEE - 302497- Procedure tray Catalog Number: ANTK12AF Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAND PACK-Procedure Kit Catalog Number: WEHD16B Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY WOLFSON PACK BHS Procedure tray Catalog Number: BPAR65A Recalled...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.