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. 1,076 recalls have been distributed to Tennessee in the last 12 months.
Showing 14081–14100 of 52,000 recalls
Recalled Item: HYDRATOME RX 49-30MM/260CM Material Number: M00583010 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors -...
The Issue: The External Retention Bolster contained in the kit may be a larger diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Philips has...
The Issue: Philips has identified a specific lot of non-conforming material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dreamtome Cannulating Sphincterotome-DREAMTOME 44-20MM/450CM Material...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Chuck-The Universal Chuck is an Instrument Handle provided as...
The Issue: Top cap may loosen and detach if the Universal Chuck becomes jammed and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL Recalled by...
The Issue: The External Retention Bolster contained in the kit may be a larger diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 49-30MM/450CM Material Number: M00584030 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Destino Twist 14F (also branded as Guidestar 14F) Recalled by Oscor Inc. Due...
The Issue: There is potential for separation between the threaded hub and threaded cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-20-260-035 Material Number: M00573000 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 44-30MM/450CM Material Number: M00584070 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME REVOLUTION RX 39-30-260-025 Material Number: M00584260 Recalled by...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 44-30MM/260CM Material Number: M00584050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-30MM/260CM Material Number: M00583050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX CHOLANGIOGRAM KIT Material Numbers: M00575241 M00575281 M00575321...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-20MM/260CM Material Number: M00583040 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-260-035 Material Number: M00573020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-450-035 Material Number: M00573030 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dreamtome RX Cannulating Sphincterotome-DREAMTOME 44-20MM/260CM Material...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 49-20MM/450CM Material Number: M00584020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250 Recalled by...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.