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. 2,676 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,676 in last 12 months

Showing 67216740 of 29,188 recalls

Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 800753005 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 880393003 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 11mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880353009 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880473001 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 800756005 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880405003 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 800718003 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 12mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 8 mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Becton Dickinson & Co.

Recalled Item: BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software Recalled by...

The Issue: Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System with software versions: R2.2.O Recalled by PHILIPS...

The Issue: Potential Loss of X-ray-When the full disk capacity is reached, X-Ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Aesculap Implant Systems LLC

Recalled Item: Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and...

The Issue: Potential for the spring to become loose and fall out of the device, if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS one with a hybrid cable- An angiography system developed Recalled by...

The Issue: Examination room monitor connected with the hybrid cable may have a display...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2023· Philips North America

Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813...

The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2023· Philips North America

Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814...

The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2023· DermLite LLC

Recalled Item: DERMLITE DL4W Recalled by DermLite LLC Due to Incorrect labeling; Package...

The Issue: Incorrect labeling; Package labeling contains a different serial number then...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Philips North America Llc

Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...

The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

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

Class II — Potential Health HazardOngoing