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. 2,485 recalls have been distributed to Oklahoma in the last 12 months.
Showing 24501–24520 of 49,976 recalls
Recalled Item: IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software...
The Issue: Quality control results are not processed for Abbott Diagnostics Alinity ci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241-S Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...
The Issue: There is a potential to generate falsely elevated serum or plasma chloride...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...
The Issue: The reagent pack exhibits the potential for an increased frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass ULTRA SYSTEM Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due...
The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due...
The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...
The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...
The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Argatroban Injection Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; Out of specification stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...
The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 Recalled by QuVa...
The Issue: Subpotent Drug: Product may not have the active ingredient present in the bag.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product...
The Issue: The Li-ion Battery Housing for the AR-400 DrillSaw Sports 400 System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Uric Acid Recalled by Beckman Coulter Inc. Due to NAPQI, a...
The Issue: NAPQI, a metabolite of Acetominophen, causes negative interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.