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. 1,110 recalls have been distributed to Tennessee in the last 12 months.
Showing 8041–8060 of 52,000 recalls
Recalled Item: Choleodochoscope. Model Numbers: CHF-BP30 Recalled by Aizu Olympus Co., Ltd....
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREXAFEMME (Ibrexafungerp) tablets 150 mg Recalled by Scynexis, Inc. Due to...
The Issue: Cross Contamination with Other Products: Potential cross-contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Penzeys Brady Street Cheese Sprinkle. Item 20756. net wt 2.2 Recalled by...
The Issue: Brady Street Cheese Sprinkle may contain sesame.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CUSTOM SPRYSTEP Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR KAFO Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of...
The Issue: Units are labeled as 10cc; however the units have a fill volume of 1cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High-Flow Insufflation Unit Recalled by Olympus Corporation of the...
The Issue: There have been reports of patients suffering arrhythmias, reported as short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest/Emergency Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713052U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi Navigation System Recalled by Acclarent, Inc. Due to When using...
The Issue: When using affected curette and software, there is a discrepancy between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Release 3 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER Recalled by Philips North America...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Release 3.1 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.