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. 2,661 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,661 in last 12 months

Showing 1146111480 of 29,188 recalls

Medical DeviceJuly 22, 2020· Smith & Nephew Orthopaedics AG

Recalled Item: POLARSTEM COLLAR Reamer Guide Recalled by Smith & Nephew Orthopaedics AG Due...

The Issue: Multiple lots being recalled due to a product design issue

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA

Recalled Item: Ezycare Face Mask Recalled by BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA...

The Issue: Disposable face masks labeled as non-medical were distributed to customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-CH EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Recalled by...

The Issue: May have one or more dimensional features out of tolerance includes: thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame Recalled by...

The Issue: Modular Junction Box (MJB) cables can melt and affect the bed functionality.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS XT7600 Integrated System Recalled by Ortho Clinical Diagnostics Due...

The Issue: When processing MicroSlides, slides that utilize Slot 18 in the CM rotor may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS XT3400 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: When processing MicroSlides, slides that utilize Slot 18 in the CM rotor may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2020· NOBEL BIOCARE SERVICES AG

Recalled Item: NobelReplace Conical Connection (CC) PMC RP 4.3x10mm Recalled by NOBEL...

The Issue: Dental implant cap label may incorrectly indicate implant measurements...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2020· Becton Dickinson & Co.

Recalled Item: BD MAX SARS-CoV-2 Reagents Recalled by Becton Dickinson & Co. Due to BD is...

The Issue: BD is experiencing elevated rates of potential false positive results from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Medtronic Neuromodulation

Recalled Item: Restore Clinician Programmer Application Software Recalled by Medtronic...

The Issue: The original version of the A71100 Restore Clinician Programmer Application...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Materialise N.V.

Recalled Item: Match Point System The Match Point System is intended to Recalled by...

The Issue: The procedure side indicated in the top header of the Shoulder Case Planning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Cytocell Ltd.

Recalled Item: Cytocell LPH533-A NUP98 Distal Probe Green - Product Usage:The NUP98...

The Issue: A low risk of a false positive result being issued with a laboratory...

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

Class II — Potential Health HazardOngoing