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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,431 in last 12 months

Showing 3934139360 of 49,976 recalls

DrugFebruary 16, 2015· West-Ward Pharmaceutical Corporation

Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corporation Due...

The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2015· Qualitest Pharmaceuticals

Recalled Item: AMLODIPINE BESYLATE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to...

The Issue: Failed tablet specifications: One lot was found to contain oversized tablets.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2015· Exactech, Inc.

Recalled Item: Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic...

The Issue: Incorrectly packaged. Outer and inner labeling may incorrectly identify the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2015· Medela Inc. EF Division

Recalled Item: - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 Recalled by...

The Issue: The firm is recalling sterile enteral feeding syringes due to determining...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2015· Aaren Scientific, Incorporated

Recalled Item: Intraocular Lens (IOL) Recalled by Aaren Scientific, Incorporated Due to...

The Issue: Aaren Scientific is recalling intraocular lenses because the instructions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodFebruary 13, 2015· Goya Foods, Inc.

Recalled Item: Kirby Black Beans Creole Seasoning Net Wt. 29 oz. Packed for Kirby Foods...

The Issue: Kirby brand black beans with creole seasoning, 29 oz. size and Goya brand...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 13, 2015· Benson's Old Home Kitchens Bakery Division

Recalled Item: Wal-Mart private label "the Bakery baked with pride Recalled by Benson's...

The Issue: Product contains undeclared allergen: Pecans.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 13, 2015· Whole Food Market

Recalled Item: Whole Foods Market "Chocolate Cake for Two" code: 246357004999 Recalled by...

The Issue: Product contains undeclared eggs.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 13, 2015· Michael Foods, Inc.

Recalled Item: Natural Shaped Fried Egg (patties) Recalled by Michael Foods, Inc. Due to...

The Issue: Improperly declared milk allergen.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 13, 2015· Goya Foods, Inc.

Recalled Item: Goya Black Bean Soup Net Wt. 29 oz. Goya Foods Recalled by Goya Foods, Inc....

The Issue: Kirby brand black beans with creole seasoning, 29 oz. size and Goya brand...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Par Pharmaceutical Inc.

Recalled Item: Mafenide Acetate Recalled by Par Pharmaceutical Inc. Due to Presence of...

The Issue: Presence of Foreign Substance; oxidized steel, organic material and shredded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Apotex Inc.

Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to CGMP...

The Issue: CGMP Deviations: Product excipient was not re-tested at the appropriate date.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging Recalled...

The Issue: Devices were not sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon...

The Issue: Potential for weld disassociation of the cross pin, which could lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...

The Issue: Devices were not sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Dako North America Inc.

Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...

The Issue: A false negative result affecting the diagnosis may occur. A defect in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing