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. 2,593 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,593 in last 12 months

Showing 1912119140 of 29,188 recalls

Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF#...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF#...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· Revision Optics Inc

Recalled Item: Raindrop Near Vision Inlay Recalled by Revision Optics Inc Due to ReVision...

The Issue: ReVision Optics has updated the instructions for use (IFU) for the Raindrop...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2017· GE Healthcare, LLC

Recalled Item: Table Patient Step on RFX/SFX Recalled by GE Healthcare, LLC Due to Reported...

The Issue: Reported incidents of a patient step detaching from the table. A fall from a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2017· Heartware

Recalled Item: HeartWare HVAD System Controller The HeartWare Ventricular Assist System...

The Issue: Product recall of all HVAD Controllers currently on the market and to...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing