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 11141–11160 of 29,188 recalls
Recalled Item: MR Coils The MR Coil is intended to be used Recalled by Invivo Corporation...
The Issue: The labels have been mistakenly printed with an IPX1 rating symbol. IPX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650301023 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650301018 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #65021652 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650600111 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #65220955 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650304917 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650305414 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #65193091 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and...
The Issue: The device may detect an incorrect Heater Bag volume which may lead to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS Software Versions 5.1 and higher Recalled by Fujifilm Medical...
The Issue: There is a potential for the wrong patient information may be displayed in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN ******* MULTIFUNCTION PEDAL OSSEODUO - Recalled by...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN ******* OSSEOSTAP Footcontrol - Product Recalled by...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS Software Version 5.6.1 - Product Usage: intended for Recalled...
The Issue: FUJIFILM has become aware of the possibility that certain CT studies may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN **** FOOTCTRL OSSEODOC - Product Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entellus Medical SN ******* Shaver System Foot Pedal Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments SN ******* S2 MINI FOOT Pedal Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System...
The Issue: When the delivery catheter was attempted to be removed, there was an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE TAG CONFORMABLE Thoracic Stent Graft with ACTIVE CONTROL System...
The Issue: Due to secondary deployment fiber being attached to secondary deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR WITH TWO Absorbable Suture anchors Recalled...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.