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. 2,710 recalls have been distributed to Tennessee in the last 12 months.
Showing 1801–1820 of 29,188 recalls
Recalled Item: Bio 1 Granules for Filling ¿ 1 mm (2 cm¿) Recalled by SCIENCE & BIO...
The Issue: Vials of implant bone granules may contain less product then specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US...
The Issue: Incorrect labeling in which the front red pouch label did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray Platte Faxitron Recalled by Klinika Mdical Gmb Due to Potential...
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray. KlinioTray. Tissue resection margin examination board/small....
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSPIRA AIR BALLOON DILATION SYSTEM 10x40 Recalled by Integra LifeSciences...
The Issue: Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Preset treatment parameters are not consistently being used in accordance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...
The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...
The Issue: Devices for the affected lot were not assembled according to product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...
The Issue: Due to manufacturing issues, abutment products were manufactured with screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HistoCore PELORIS 3 Recalled by Leica Biosystems Melbourne Pty Ltd Due to...
The Issue: There is a leakage issue associated with the tubing in the manifold of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: myQA iON Recalled by IBA Dosimetry GmbH Due to Wrong analysis results can...
The Issue: Wrong analysis results can occur if the user creates two structures with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Brilliance CT Big Bore Recalled by Philips North America Llc Due to...
The Issue: Unintended motion issues related to Interventional Control that may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72...
The Issue: During routine preventative maintenance checks, it was revealed that carbon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit Recalled...
The Issue: An issue with a raw material used to coat some surgical needles that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.