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. 2,379 recalls have been distributed to Oklahoma in the last 12 months.
Showing 46581–46600 of 49,976 recalls
Recalled Item: (No Brand) First Aid Kit Recalled by Total Resources Intl Due to CGMP...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medi-First Brand First Aid Kit Recalled by Total Resources Intl Due to CGMP...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by Aurobindo Pharma USA Inc Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength: Incorrect strength on side...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an...
The Issue: Several complaints were recorded regarding one of the three screws driving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalight 80 Model Number UVB-080 Recalled by National Biological Corp Due...
The Issue: The incorrect manual may have been packaged with this product. UVB-080...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL RecombiPlasTin 2G Recalled by Instrumentation Laboratory Co. Due to...
The Issue: Instrumentation Laboratory is recalling HemosIL RecombiPlasTin 2G (RPT2G),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neurology Dantec KEYPOINT.NET 2.20. Catalog/Part Numbers: 9031A070103...
The Issue: Alpine Biomed ApS is recalling Natus neurology Dantec KEYPOINT.NET ver. 2.20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was identified...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Endopath Electrosurgery Probe Plus II Recalled by Ethicon Endo-Surgery Inc...
The Issue: The firm is recalling the ENDOPATH Probe Plus II Shafts because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defribillator Recalled by Philips Healthcare Inc. Due...
The Issue: Device may fail to deliver defibrillation therapy in either Manual Defib or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glenmark Gabapentin Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Gabapentin Sodium tablets is recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Pravastatin Sodium Tablets Recalled by Glenmark Generics Inc., USA...
The Issue: Chemical Contamination: Pravastatin Sodium Tablets isbeing recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Topiramate Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Topiramate Tablets is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROFILE-V MEDTOXScan Drugs of Abuse Test System. For the rapid Recalled by...
The Issue: Review of validation information and customer complaints which indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.