Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,535 in last 12 months

Showing 2254122560 of 29,188 recalls

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 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· GE Healthcare

Recalled Item: GE Healthcare Precision RXi Digital system Recalled by GE Healthcare Due to...

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 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· Oxysure Systems, Inc.

Recalled Item: OxySure Model 615 disposable replacement cartridges Recalled by Oxysure...

The Issue: Flow rate of the recalled replacement cartridges does not meet the draft FDA...

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· 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 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· 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· 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· 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· CryoLife, Inc.

Recalled Item: On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement...

The Issue: Incorrect product label. The type of Sewing Ring was mislabeled as being a...

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 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· 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· Synthes (USA) Products LLC

Recalled Item: Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA)...

The Issue: The height of one of the three guiding pins of the Helical Blade Inserter...

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
Medical DeviceJune 9, 2015· Omnilife Science Inc.

Recalled Item: Offset Femoral Alignment Guide Recalled by Omnilife Science Inc. Due to The...

The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2015· Olympus Scientific Solutions Americas

Recalled Item: Olympus Scientific Solutions Americas Analytical X-ray System. Delta...

The Issue: Higher than published scatter around the probe head when testing some...

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

Class II — Potential Health HazardOngoing