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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.
Showing 18541–18560 of 49,976 recalls
Recalled Item: Type S Extension For use with Varian Recalled by Med Tec Inc Due to...
The Issue: Potential for disengagement of the Varian Style Type-S Extension during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) + Curcumin 50mg/mL Recalled by BIOTA Biosciences...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Curcumin 50mg/mL Recalled by BIOTA Biosciences LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Curcumin Recalled by BIOTA Biosciences LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) 4mg/mL Recalled by BIOTA Biosciences LLC Due to...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) 50mg/mL Recalled by BIOTA Biosciences LLC Due to...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ABL80-FLEX CO-OX 393-841 Box Label Recalled by Radiometer Medical ApS Due to...
The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...
The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product Performance Verifier I Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product Performance Verifier II Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...
The Issue: The product is being recalled due to the central screw drill seizing inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...
The Issue: Presence of Particulate Matter: confirmed customer complaint for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...
The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...
The Issue: An error in the calculation of the Michigan Ranges can generate an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Compression Screw Recalled by Stryker GmbH Due to Seal integrity of...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.