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. 2,072 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,072 in last 12 months

Showing 70017020 of 52,000 recalls

Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.3.000 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
FoodJanuary 10, 2024· Now Foods

Recalled Item: Protocol for Life Balance Recalled by Now Foods Due to Amount of...

The Issue: Amount of Phosphatidyl Serine in product is less than stated on the label

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugJanuary 10, 2024· BE PHARMACEUTICALS AG

Recalled Item: Fosaprepitant for Injection 150 mg per vial Recalled by BE PHARMACEUTICALS...

The Issue: Lack of Sterility Assurance: Aseptic process simulation failure.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Remedy Clinical TREAT Antifungal Cream Recalled by MEDLINE...

The Issue: Labeling: Not Elsewhere Classified; Product labeling contains the claim of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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· 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· Aesculap Inc

Recalled Item: DISP.HASSON TROCAR 12/110MM Recalled by Aesculap Inc Due to The sterile...

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 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· 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· 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· Aesculap Inc

Recalled Item: DISP.HASSON TROCAR 10/110MM Recalled by Aesculap Inc Due to The sterile...

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: Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis Recalled...

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· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" Recalled by...

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· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL Recalled by...

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· 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· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL Recalled by...

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· 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