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. 2,504 recalls have been distributed to Tennessee in the last 12 months.
Showing 25781–25800 of 29,188 recalls
Recalled Item: Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Recalled...
The Issue: As part of routine manufacturing process monitoring by Zimmer, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel 4# Disposable...
The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008 Series Hemodialysis Machines: Models: 2008H Recalled by...
The Issue: 2008 Series Hemodialysis Machines complaints of saline bags inappropriately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Long Disposable...
The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Advanced Energy Aquamantys3 Pump Generator Recalled by Medtronic...
The Issue: The internal protection circuitry on the electrosurgical output that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Recalled by Advanced Sterilization Products Due to Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunrise Brand Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to...
The Issue: There is a remote possibility for the plastic latch to deform over the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assembly Recalled by Intuitive Surgical, Inc. Due to Reports of friction...
The Issue: Reports of friction within certain instrument arms can interrupt smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Recalled by Advanced Sterilization Products Due to Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria () API Listeria is a standardized system Recalled by Biomerieux...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Monitor Suspensions that may be on the following Fluoroscopic Recalled...
The Issue: Missing screws in the overhead Video Monitor Suspension. GE discovered that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 750 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaSafe Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the VersaSafe Extension Intravascular Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 780 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FastPack Testosterone Immunoassay Chemilunescence assay for the...
The Issue: Qualigen initiated this recall because the FastPack kit may cause lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NH () API NH is a standardized system Recalled by Biomerieux France...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent () ZYM B reagent is an Recalled by Biomerieux France Chemin De...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FastPack Total PSA Immunoassay Chemilunescence assay for the determination...
The Issue: Qualigen initiated this recall because the FastPack kit may cause lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB) Recalled by Arrow...
The Issue: Potential for a leak between the catheter and the bifurcate which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FastPack Free T4 Immunoassay FastPack Vitamin D Immunoassay Chemilunescence...
The Issue: Qualigen initiated this recall because the FastPack kit may cause lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.