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. 936 recalls have been distributed to Oklahoma in the last 12 months.
Showing 47121–47140 of 49,976 recalls
Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: There is a potential for the solution to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAXILOSS Weight Advanced Recalled by OLAAX International Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: product contains sibutramine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...
The Issue: Out of specification result - stability test failure of free available...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...
The Issue: Philips was notified of a problem using the IntelliSpace Portal with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization Recalled...
The Issue: The control boards alarm set points and temperature tolerances allowed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...
The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....
The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...
The Issue: Multiple incidents of low-reacting assay plates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed Release Tablets USP Recalled by Jubilant Cadista...
The Issue: cGMP Deviations: Oral products were not manufactured in accordance with Good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meprobamate Recalled by Watson Laboratories Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meprobamate Recalled by Watson Laboratories Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...
The Issue: Orthodontic brackets distributed was incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.