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. 2,452 recalls have been distributed to Tennessee in the last 12 months.
Showing 38141–38160 of 52,000 recalls
Recalled Item: Imperial Sugar Recalled by Savannah-Imperial LP- Savannah Sugar Due to...
The Issue: Foreign matter (blue fiber) detected in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clear Value Sugar Recalled by Savannah-Imperial LP- Savannah Sugar Due to...
The Issue: Foreign matter (blue fiber) detected in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Imperial GMI Recalled by Savannah-Imperial LP- Savannah Sugar Due to Foreign...
The Issue: Foreign matter (blue fiber) detected in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Laura Lynn Recalled by Savannah-Imperial LP- Savannah Sugar Due to Foreign...
The Issue: Foreign matter (blue fiber) detected in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: West Creek Recalled by Savannah-Imperial LP- Savannah Sugar Due to Foreign...
The Issue: Foreign matter (blue fiber) detected in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Recalled by Savannah-Imperial LP- Savannah Sugar Due to Foreign...
The Issue: Foreign matter (blue fiber) detected in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CooperSurgical LEEP REDIKIT-Used as a surgical preparatory kit for Loop...
The Issue: Kit Label incorrect :Labeled with Lidocaine HCI drug cartridges Lidocaine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Recalled by AGFA Healthcare Corp. Due to Customers have experienced...
The Issue: Customers have experienced IMPAX CV software, specifically, Demographics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...
The Issue: An issue with a USB memory component contained within a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caramel Caribou Ice Cream Recalled by The Ice Cream Club, Inc. Due to...
The Issue: Product contains undeclared peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fujifilm Medical Systems Duodenoscope Recalled by Fujifilm Medical Systems...
The Issue: A precautionary measure because the Duodenoscopes have been redesigned to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.