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. 2,638 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,638 in last 12 months

Showing 1352113540 of 29,188 recalls

Medical DeviceJuly 26, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Surgical System Recalled by Intuitive Surgical, Inc. Due to The...

The Issue: The firm become aware of a potentially defective capacitors on circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2019· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed Carestation CS1 - Product Usage: The device can Recalled by...

The Issue: Fasteners potentially torqued to a value less than the specified value and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Randox Laboratories Ltd.

Recalled Item: Randox Urinalysis Control Level 2 (IVD) - Product Recalled by Randox...

The Issue: Analyte range for Leukocytes for use with the Siemens Multistix method is...

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

Class III — Low RiskOngoing
Medical DeviceJuly 25, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed...

The Issue: SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrig ETF Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Push Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endintrak 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity of...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endintrak¿ 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Push Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: WS80A Diagnostic Ultrasound System Version 1.00.16 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: HS70A Diagnostic Ultrasound System Version 2.01.00 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2019· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc. Due to...

The Issue: Potential for Hemospray device to be unable to spray powder due to...

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

Class II — Potential Health HazardOngoing