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. 2,670 recalls have been distributed to Tennessee in the last 12 months.
Showing 8521–8540 of 29,188 recalls
Recalled Item: 3.2MM Pellet Insertion Tray Catalog Number: B7345R1 Recalled by Busse...
The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I.V. Start Kit - Tegaderm Dressing - Catheter Securement - Recalled by Busse...
The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MBB Tray Catalog Number: 9882 Recalled by Busse Hospital Disposables, Inc....
The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural Tray Catalog 1577 Recalled by Busse Hospital Disposables, Inc. Due...
The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SS 3.5MM Diamond Tip Trocar - Large Gloves Catalog Number: B1547 Recalled by...
The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Shot Epidural Tray Catalog 1165 Recalled by Busse Hospital...
The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Male SS 4.5MM Pellet Insertion Tray Catalog Number: B9176R1 Recalled by...
The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems HCG [200 Tests Recalled by Siemens Healthcare...
The Issue: Potential for falsely elevated hCG results due to sample carryover in serum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 300 CTS/350 CTS/500 CTS/550 CTS/970 CL: Name Part Recalled by...
The Issue: Updated and revised user instructions issued 7/14/22. Potential carryover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illumina NextSeq 550Dx Recalled by Illumina, Inc. Due to There is a...
The Issue: There is a potential that the DNA sequence analyzer may short circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm Recalled by...
The Issue: Due to failure of microbial testing for total aerobic microbial count (TAMC).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Universal Twinbar 670 QRH Recalled by Baxter Healthcare Corporation Due...
The Issue: An incorrect center bolt was used in the assembly of the product which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems...
The Issue: Potential for false positive results for SARS-CoV-2 in identified lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORAcollect RNA: ORE-100 Recalled by DNA Genotek Inc. Due to Evaporation of...
The Issue: Evaporation of stabilizing liquid reducing shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORAcollect Dx Recalled by DNA Genotek Inc. Due to Evaporation of stabilizing...
The Issue: Evaporation of stabilizing liquid reducing shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signa 1.5T TwinSpeed Magnetic Resonance Imaging System Recalled by GE...
The Issue: There is potential for the images to be flipped left to right.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Excite 3T. Magnetic Resonance Imaging System Recalled by GE...
The Issue: There is potential for the images to be flipped left to right.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T SIGNA Excite HD Recalled by GE Healthcare, LLC Due to There is...
The Issue: There is potential for the images to be flipped left to right.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T and 3.0T SIGNA HDx Recalled by GE Healthcare, LLC Due to There is...
The Issue: There is potential for the images to be flipped left to right.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp-i Transport Guard with Transport Guard (701072525): is a blood...
The Issue: Potential for a loose cylindrical pin on the Transport Guard that may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.