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. 2,509 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,509 in last 12 months

Showing 2452124540 of 29,188 recalls

Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 101 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Adaptor Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Excelsior Medical Corp

Recalled Item: Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Recalled...

The Issue: There is a potential for a leak. A molding defect in the connector that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Humidifier Adaptor 040 Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aqua 540 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the respiratory gas humidifier adaptor packaging may be creased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak SW/EAU Sterile Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Briggs Medical Service Company d.b.a. Mabis

Recalled Item: DMI Duro-Med Industries Rollator Transport Chair Recalled by Briggs Medical...

The Issue: There have been 5 customer reports of a 501-1018 series DMI Rollator...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...

The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Humidifier Adaptor Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak SW/EAU Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing