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. 2,664 recalls have been distributed to Tennessee in the last 12 months.
Showing 10961–10980 of 29,188 recalls
Recalled Item: Mako Integrated Cutting System (MICS) Handpiece Recalled by Mako Surgical...
The Issue: Stryker has discovered a characterization issue associated with the Mako...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to Some...
The Issue: Some electronic components within the generator were equipped with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpen Clinic 100 Carbide Instruments (R100057C) Recalled by Coltene...
The Issue: The FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewRay MRIdian System: Model No. 10000 Recalled by Viewray, Inc. Due to...
The Issue: There is a potential that components of the receive coil can reach elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewRay MRIdian Linac System: Model No. 20000 Recalled by Viewray, Inc. Due...
The Issue: There is a potential that components of the receive coil can reach elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEI Cutting Edge Instruments (PTC-57C) Recalled by Coltene Whaledent Inc Due...
The Issue: The FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FG 57 100057X (100057X) Recalled by Coltene Whaledent Inc Due to The FG 557...
The Issue: The FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinic Pack 100 Pieces FG 57 100057C (100057C) Recalled by Coltene Whaledent...
The Issue: The FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strauss 25 Carbide Dental Burs (100057XXV) Recalled by Coltene Whaledent Inc...
The Issue: The FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone Recalled by...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Treatment beam...
The Issue: Treatment beam information disappears on Treatment Console screen while beam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone Recalled...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone Recalled...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.