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 2566125680 of 28,654 recalls

Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...

The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Mesa Laboratories, Inc.

Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...

The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· CooperSurgical, Inc. D.B.A. Lone Star Medical Products

Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...

The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Southern Implants, Inc

Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...

The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....

The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Maquet Medical Systems USA

Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...

The Issue: It has come to the attention of MAQUET that in certain rare instances, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...

The Issue: There is a potential issue on running Artis systems running software VC1x...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· ArjoHuntleigh Inc.

Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...

The Issue: The lock pin can become stuck in the "in" position during the manual...

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

Class II — Potential Health HazardOngoing