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 18921–18940 of 49,976 recalls
Recalled Item: Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel Hydrogel 4oz. Tube. Wound dressing containing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel 4"x4" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...
The Issue: Failed impurities/degradation specification: Out-of-Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xience Sierra TM Everolimus Eluting Coronary Stent System Recalled by Abbott...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tetracycline HCL Capsules Recalled by Avet Pharmaceuticals, Inc. Due to...
The Issue: Failed Dissolution Specifications: Out of specification result during long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tetracycline HCL Capsules Recalled by Avet Pharmaceuticals, Inc. Due to...
The Issue: Failed Dissolution Specifications: Out of specification result during long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tacrolimus Capsules Recalled by Mylan Pharmaceuticals Inc. Due to Presence...
The Issue: Presence of foreign tablet/capsule - Potential presence of commingled one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/...
The Issue: The hemostasis valve of aspiration guide catheter devices may fail to seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is Recalled...
The Issue: It was identified that there is a potential for the Stim Interconnecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for...
The Issue: It was identified that there is a potential for the Stim Interconnecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...
The Issue: There was no data to validate that the identified endo-therapy devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...
The Issue: There was no data to validate that the identified endo-therapy devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre 5F Plus Over the Wire Embolectomy Catheter Recalled by LeMaitre...
The Issue: There has been an increased trend in reports of catheters failing to deflate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUANGFUSHANZHEN Recalled by Tiffany Food Corp. Due to Undeclared Sulfites
The Issue: Product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Utak NR Trace Elements Serum Control Recalled by Utak Laboratories Inc Due...
The Issue: The product has an incorrect value for cadmium and an incorrect expected range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifePAK 500 Automated External Defibrillator Recalled by Physio-Control,...
The Issue: Automated External Defibrillators may not detect a patient connection due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftazidime Sterile Ophthalmic Solution for Injection Preservative Free...
The Issue: Lack of Assurance of Sterility; the media used to conduct post-compounding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Recalled by Edge Pharma, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility; the media used to conduct post-compounding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.