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 8521–8540 of 29,188 recalls
Recalled Item: I.V. Start Kit Catalog 8172 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: Port Tray Catalog 7607 Recalled by Busse Hospital Disposables, Inc. Due to...
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: Sterile Epidural Tray Catalog Number: 6259R2 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: SS 3.5Mm Pellet Insertion Tray with large Gloves Catalog Number: B1352R1...
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: "3.2MM Pellet Insertion Tray with Medium Gloves" Catalog Number: B1351...
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: 4.5 MM Pellet Insertion Tray Catalog Number: B8121R1 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: Single Shot Epidural Tray Catalog Number: 6183R1 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: Nerve Block Tray Catalog Number: 3764R2 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: Universal Nerve Block Tray Catalog Number: 9818 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: Lumbar Tray Catalog 1091 Recalled by Busse Hospital Disposables, Inc. Due to...
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: 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: 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: Medical Device products purchased from Family Dollar retail stores located...
The Issue: Potential exposure to rodents and rodent activity in the distribution center.
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 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: 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.
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: 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: 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.