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. 2,580 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,580 in last 12 months

Showing 1940119420 of 29,188 recalls

Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Blood Recovery Drains as follows: 3650-100 Oasis...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical 16400 Express Mini 500 dry seal drain Product Recalled by...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical 400 Series Express Drains as follows: 4000-100N Express...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Ocean Blood Recovery Drains as follows: 2050-000 Ocean...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: CentraLink¿ Data Management System Software Versions: v13x Recalled by...

The Issue: There is a remote possibility CentraLink may download an order to the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes VA Implant Rack for the Compact Distal Radius System Recalled by...

The Issue: The screw rack plate was assembled incorrectly which could cause the screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Single Drain as follows: 3600-100 Oasis single Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Pediatric Chamber Ocean Drains as follows: 2012-320 Ocean...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Sekisui Diagnostics P.E.I. Inc.

Recalled Item: Sekisui Diagnostics Ammonia L3K¿ Assay Recalled by Sekisui Diagnostics...

The Issue: Certain lots are showing an atypical decrease in optical density (OD) over...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Ocean Drains as follows: 2002-000 Ocean single drain Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Xcela PICC Kit with ENDEXO and PASV Valve Technology Recalled by...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG Recalled by Angiodynamics...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Valved PG Recalled by Angiodynamics Inc....

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: XCELA PASV 5F DL 55CM IR-145 Nitinol Wire KIT PG Recalled by Angiodynamics...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Valved PG Recalled by Angiodynamics Inc....

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Cook Inc.

Recalled Item: Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous...

The Issue: Cook Medical has received reports of the trays containing the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved w/ Nit GW Recalled by...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG Recalled by Angiodynamics...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Valved with Nit GW Recalled by...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing