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. 2,580 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,580 in last 12 months

Showing 2012120140 of 29,188 recalls

Medical DeviceAugust 2, 2016· Becton Dickinson & Company

Recalled Item: catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 Recalled by Becton...

The Issue: A recall was initiated by Hospira, Inc. for several lots of 5% Lidocaine HCI...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Alere San Diego, Inc.

Recalled Item: LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Recalled...

The Issue: Incorrect expiration date on the magnetic strip that does not match the...

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

Class III — Low RiskOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion Stationary X-Ray System Product Usage: The Multix Fusion...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Ethicon, Inc.

Recalled Item: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Recalled by...

The Issue: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Strip or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Patella Assembly Instrument Recalled by Stryker...

The Issue: Upon failure of the press-fit, the clamping sub components and pins could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO Max Product Usage: The Ysio Max is a radiographic Recalled by Siemens...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion VA10 Product Usage: The Multix Fusion VA10 system Recalled by...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· B. Braun Medical, Inc.

Recalled Item: Sterile IV Start Kits 50 units/trays per case Convenience kit Recalled by B....

The Issue: Positive results from non-routine sterility testing commissioned by B. Braun...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Sterile. Rx For Use with Zyno Recalled by...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products TSH Reagent Pack Recalled by ORTHO-CLINICAL...

The Issue: A field correction was issued by the firm for VITROS TSH reagent lot 5040...

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

Class III — Low RiskOngoing
Medical DeviceJuly 27, 2016· INNOKAS MEDICAL OY

Recalled Item: CARESCAPE VC150 Vital Signs Monitor Recalled by INNOKAS MEDICAL OY Due to A...

The Issue: A software error on released software versions 1.6.12, 1.6.12F and 1.6.16...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing