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. 1,076 recalls have been distributed to Oklahoma in the last 12 months.
Showing 13301–13320 of 49,976 recalls
Recalled Item: 70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen Recalled by Tsm...
The Issue: Labeling - product contains undeclared ethyl alcohol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Topical Gel USP Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Lot not meeting specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorthalidone Tablets USP 25 mg Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: Foreign Matter identified as stainless steel microscopic wear particles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Chewable Tablets Recalled by RISING...
The Issue: Failed Tablet Specifications: Recall of this drug product was voluntarily...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jaguar Power Honey packaged in a gold paper box with black writing Recalled...
The Issue: Contains hidden drug ingredient
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Helmi Honey VIP packaged in a gold paper box with black writing Recalled by...
The Issue: Contains hidden drug ingredient
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Maxi Swabstick...
The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MegMan Performance Booster Recalled by Junp Hydration LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PARAGARD T380A (intrauterine copper contraceptive) Recalled by...
The Issue: Non-sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swab Recalled by...
The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick...
The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System software version2.8.0 Recalled by Abbott Laboratories, Inc...
The Issue: Software error associated with the immunoassay analyzer wash cycle which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit catalog # 76645 & 73806 Recalled by Terumo...
The Issue: Potential for Cardiovascular Procedure Kit packaging damage that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller)...
The Issue: Multi-Modality Touch Screen Modules (MM-TSM), used with integrated IVUS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura (Model Numbers 722010 Recalled by Philips North America Llc...
The Issue: Due to a software defect, the Philips StentBoost Live R2.0 might not process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips StentBoost Live R2.0 application Recalled by Philips Healthcare Due...
The Issue: Due to an incorrect configuration setting in the EPX database of StentBoost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.