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. 2,638 recalls have been distributed to Tennessee in the last 12 months.
Showing 14001–14020 of 29,188 recalls
Recalled Item: InterStim(TM) System Recalled by Medtronic Neuromodulation Due to There is a...
The Issue: There is a potential for an unexpected increase in stimulation during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntraClude Intra-Aortic Occlusion Device Recalled by Edwards Lifesciences,...
The Issue: Possibility of balloon rupture in intra-aortic occlusion devices. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST- Amber Part/Catalog Number: 365978 Recalled by Becton...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST Part/Catalog No.365967 Recalled by Becton Dickinson &...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cadence Science Pressure Control Glass Syringe Recalled by Cadence Science,...
The Issue: The glass syringe used with Pressure Control Syringes may potentially break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated...
The Issue: Reported complaints of cracks being observed, prior to use, on swivel wye...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA RF IgM Well Recalled by Phadia Ab Due to Potential for reporting low...
The Issue: Potential for reporting low assay results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leadwire sets with snap ends: REF/Catalog Number Description 2106381-001 ECG...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement leadwires with grabber ends: REF/Catalog Number Description...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECG Trunk Cables: REF/Catalog Number Description 2106305-001 ECG Trunk Cable...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement ECG leadwires with snap ends REF/Catalog Number Description...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioCommand Recalled by Cardiocommand Inc. Due to Possible corrosion of...
The Issue: Possible corrosion of the battery contact(s).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rim Plate Recalled by I.T.S. GmbH Due to The titanium implant has the wrong...
The Issue: The titanium implant has the wrong article number laser marked on it.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.