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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,468 in last 12 months

Showing 2772127740 of 49,976 recalls

Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
DrugOctober 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Dutasteride and Tamsulosin HCl Capsules Recalled by Teva Pharmaceuticals USA...

The Issue: Failed dissolution specifications; all lots within expiry are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2017· Fagron, Inc

Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...

The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2017· Amerisource Health Services

Recalled Item: Paroxetine Tablets Recalled by Amerisource Health Services Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lat Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Radial Head Assy Size #3 Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Radial Head Assy Size #2 Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Medacta Usa Inc

Recalled Item: The GMK knee system: designed for cemented use in total Recalled by Medacta...

The Issue: Medacta has observed a worldwide occurrence rate of post-operative insert...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: radial head implant #2 (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lat Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: radial stem implant #2 (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing