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. 2,694 recalls have been distributed to Tennessee in the last 12 months.
Showing 4041–4060 of 29,188 recalls
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Model Number (REF): (1) 781345 Recalled by Philips North...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR system 1.5T Marlin- Magnetic Resonance (MR) systems are Medical Recalled...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S Model Number (REF): (1) 782139 Recalled by Philips North...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X- Magnetic Resonance (MR) systems are Medical Electrical...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 3.0T Model Number (REF): 782145 Recalled by Philips...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution upgrade 3.0T Model Number (REF): (1)782117 Recalled by Philips...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.