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. 2,547 recalls have been distributed to Tennessee in the last 12 months.
Showing 20221–20240 of 29,188 recalls
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...
The Issue: The STAT priority icon was not displayed in the Study List when the study...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quattro Air FFM MED AMER Recalled by Resmed Corporation Due to Masks in...
The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...
The Issue: Software malfunction; The action being taken due to the device becoming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED Recalled by Bausch & Lomb Inc...
The Issue: Possible dull knife edge
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to...
The Issue: Possible dull knife edge
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to The product contained a...
The Issue: The product contained a latex catheter instead of a silicone catheter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Option-vm Urinary Catheter. Male use only. Latex Free. Sterile Recalled by...
The Issue: During an FDA inspection it was found out that the Practical Foley Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Option-vf Urinary Catheter. Female use only. Latex Free. Sterile Recalled by...
The Issue: During an FDA inspection it was found out that the Practical Foley Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432 Recalled...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....
The Issue: The product lot failed to meet QC acceptance criteria during stability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.