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. 2,553 recalls have been distributed to Oklahoma in the last 12 months.
Showing 19261–19280 of 49,976 recalls
Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...
The Issue: GMP Deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Truliant Splined Stem Extension Recalled by Exactech, Inc. Due to These...
The Issue: These Truliant Splined Stem Extension, 18mm x 120mm were found to have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans...
The Issue: FridaBaby has been made aware through customer reports that the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solifenacin Succinate Tablets Recalled by Breckenridge Pharmaceutical, Inc...
The Issue: CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Solifenacin Succinate Tablets Recalled by Breckenridge Pharmaceutical, Inc...
The Issue: CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olmesartan Medoxomil Tablets 20 mg Recalled by Ascend Laboratories LLC Due...
The Issue: cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pioglitazone and Metformin Hydrochloride Tablets Recalled by Macleods Pharma...
The Issue: Subpotent Drug: Out of specification assay result, below specification, for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply...
The Issue: The recall has been initiated due to potential for overheating or a fire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LN 3R70-01 Recalled by Abbott Gmbh & Co. KG Due to Abbott has identified...
The Issue: Abbott has identified potential performance issues for the Alinity ci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000...
The Issue: Potential exists for one or more axes of the robotic stand to become blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Recalled by Ra...
The Issue: A software issue was identified which could result in user or patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minocycline Hydrochloride Extended-Release Tablets Recalled by Ascend...
The Issue: Failed Dissolution Specifications: low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triton Canister System (finished part numbers FG 12009 Recalled by Stryker...
The Issue: Some Canister Scanning Labels used to calibrate the Triton Canister System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical, Cardiac Rhythm Management Division Due...
The Issue: Past updates to programmers and transmitters may lead some implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Dietary Supplement manufactured and distributed by ABH Nature's Products...
The Issue: Firm ordered by consent decree to recall all products because the products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.