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. 2,392 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,392 in last 12 months

Showing 4422144240 of 49,976 recalls

Medical DeviceOctober 16, 2013· Baxter Healthcare Corp.

Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...

The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...

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

Class II — Potential Health HazardOngoing
DrugOctober 16, 2013· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ciclopirox Shampoo 1% Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Subpotent. drug

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2013· B. Braun Medical Inc

Recalled Item: Cefepime for Injection USP and Dextrose Injection USP Recalled by B. Braun...

The Issue: Presence of Particulate Matter: The 1g Cefepime for Injection USP and...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 15, 2013· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension USP 125mg/5mL Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: A lidding deformity allowed for the product to have out...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...

The Issue: One material batch used for production of the affected parts of the Synthes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Teleflex Medical

Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Radiometer America Inc

Recalled Item: ABL90 FLEX Analyzer Radiometer Medical ApS Recalled by Radiometer America...

The Issue: RADIOMETER become aware that if the ABL90 FLEX is tilted, this may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...

The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Healthcare Informatics, Inc.

Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...

The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...

The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· BioMerieux SA

Recalled Item: VIDAS TPSA Recalled by BioMerieux SA Due to Product is not approved or...

The Issue: Product is not approved or authorized for distribution in the US.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: HERBERT BONE SCREW Recalled by Zimmer, Inc. Due to Zimmer recently conducted...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA Recalled by Zimmer, Inc....

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 1.5 X 6 CORT SCREW HEX/SE 2.0 X 6 CORT Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing