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. 2,536 recalls have been distributed to Tennessee in the last 12 months.
Showing 21301–21320 of 29,188 recalls
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for...
The Issue: The DX-D100 User Manual already contained information about to move a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit Recalled by Magellan Diagnostics, Inc. Due...
The Issue: LeadCare II Test Kits controls out of range
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits from Centurion that contain an In-Vision- Plus Needleless...
The Issue: Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI H/S Cuvette Recalled by Sorin Group USA, Inc. Due to The CDI System 500...
The Issue: The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeaterBaum Foot & Ankle Heating Pad Recalled by Ergoactives, Llc Due to...
The Issue: Products are marketed without a cleared 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Picture Archiving and Communication System (PACS) intended to display...
The Issue: To inform users about the possible incorrect values for Distance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile wDR motorized portable diagnostic X-ray systems. Intended for use...
The Issue: This is related to previous 806 Notifications about uncommanded movements of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics Due to Software Issue
The Issue: Software Issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HEMI STEPPED Recalled by Smith & Nephew, Inc. Due to The package...
The Issue: The package for catalog item, a LEGION Hemi Stepped Tibial Wedge, 5 MM Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jadak Barcode Scanner Recalled by CareFusion 303, Inc. Due to Customers...
The Issue: Customers reported issues when scanning medications with the scanners. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Battery Charger II (UBC II) Recalled by The Anspach Effort, Inc....
The Issue: The device is reported to enter safe mode and is no longer able to charge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.