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 2006120080 of 52,000 recalls

Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Telescopic Uncoated (Push Button) Recalled by Stryker Instruments Div. of...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Philips North America, LLC

Recalled Item: Philips DigiTrak XT Holter Recorder Software version number B.1 and Recalled...

The Issue: if an AAA battery is inserted in the recorder and a user attempts to start...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· CooperVision Inc.

Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Recalled by...

The Issue: Incorrect power of lenses than the expected

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· CooperVision Inc.

Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft...

The Issue: Incorrect power of lenses than the expected

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: DP-30 Digital Ultrasonic Diagnostic Imaging System Recalled by Mindray DS...

The Issue: The DP-30 displays an incorrect needle-guide bracket when used with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: SafeAir Telescopic Smoke Evacuation Pencil Recalled by Stryker Instruments...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· C.R. Bard Inc

Recalled Item: The Bard Intra-abdominal Pressure Monitoring Device is composed of a...

The Issue: Leaks or disconnect near the sampling port of the Intra Abdominal Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Telescopic Smoke Evac Pencil Recalled by Stryker Instruments Div. of Stryker...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Reaction Ring Segment Recalled by Siemens Healthcare...

The Issue: Some lots ending in "17", "18", "19", or higher may have cuvette defects...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRNF SURG GOWN L 2 TOWELS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABREINF SURG GOWN LARGE Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABREINF SURG GOWN L NS Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: GOWN SURG LG W/TOWEL ST BACK Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: ROYALSILK XLARGE Recalled by Cardinal Health Due to The gowns contain an...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: ROYALSILK 2XLARGE Recalled by Cardinal Health Due to The gowns contain an...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NON-REINF SURG GOWN 2XL BNS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRNF SURG GWN XL 2 TOWELS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 ROYALSILK SURGGOWN BNS L Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: ROYALSILK 3XLARGE/XLONG NS Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONREINF SURGICAL GOWN 4XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing