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. 2,690 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,690 in last 12 months

Showing 48814900 of 29,188 recalls

Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.TROCAR W. DILATING PIN 10/110MM Recalled by Aesculap Inc Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Covidien

Recalled Item: Medtronic Invos Recalled by Covidien Due to manufacturing defects to sensor...

The Issue: manufacturing defects to sensor cable connectors may result in error codes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Dr Franz Koehler Chemie Gmbh

Recalled Item: Custodiol HTK Solution Recalled by Dr Franz Koehler Chemie Gmbh Due to...

The Issue: Potential for particles to be present in solution.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Covidien

Recalled Item: Medtronic Invos Recalled by Covidien Due to manufacturing defects to sensor...

The Issue: manufacturing defects to sensor cable connectors may result in error codes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Ciprofloxacin- 5 ug Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefixime - 5 ug¿ Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Aztreonam - 30 ug¿ Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Microbiologics Inc

Recalled Item: Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet) Recalled...

The Issue: The negative control was contaminated with one of the positive control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Augmentin - 3¿g Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing