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.

49,976 total recalls
2,485 in last 12 months

Showing 2218122200 of 28,654 recalls

Medical DeviceJune 12, 2015· BioMerieux SA

Recalled Item: Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro...

The Issue: QC results were out of range resulting in false resistant strains.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and...

The Issue: The SFD/IDD safety mechanism may not engage properly at the lower range of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV FB PS ARTICULATION SURFACE SZ1-10 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Precision RXi 23A/32A Analog System Recalled by GE Healthcare...

The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE RP CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE RP PS ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED Recalled by DePuy Orthopaedics,...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE FB CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV RP PS TB TRL SZ10 INTENDED USE: The Recalled by DePuy...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV RP CR ARTICULATION SURFACE SZ1 Recalled by DePuy Orthopaedics,...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV FB CR ARTICULATION SURFACE SZ1 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A reported incident of a...

The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV RP PS ARTICULATION SURFACE SZ1-9 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Precision 500D Classical R & F system. Recalled by GE...

The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Justright Surgical, LLC

Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...

The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Abbott Laboratories

Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...

The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Justright Surgical, LLC

Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...

The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2015· Northern Digital Inc.

Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...

The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...

The Issue: There is a potential issue that could result to collision between the C-arm...

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

Class II — Potential Health HazardOngoing