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. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 27561–27580 of 29,188 recalls
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 1 inch Coated Blade with...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: HeartWare, Inc. of Miami Lakes, FL is recalling their Ventricular Assist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...
The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Needle Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 4 inch Coated Blade Recalled...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUR/Endoscopic Cable Recalled by ConMed Corporation Due to ConMed received...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet ELS Cannula 15 FR. Used for extracorporeal membrane oxygenation...
The Issue: ELS 15 Fr Cannula could potentially contain an occluded arterial lumen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle...
The Issue: BacT/ALERT SA Culture Bottle lot 1031866 may contain bottles with uncured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1-DAY ACUVUE MOIST Brand Contact Lenses Recalled by Johnson & Johnson Vision...
The Issue: Limited number of individual contact lens packages may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD¿ Composite Series Base Unit Standard Recalled by Integra...
The Issue: Integra determined there is a possibility that the Base Units may break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...
The Issue: Limited number of individual contact lens packages may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicBrainEX Product Usage: nordicBrainEx is an image processing software...
The Issue: There is an error related to the relative geometry between fiber tracts in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate Balloon Guide Catheter Recalled by Concentric Medical Inc Due to...
The Issue: Firm received complaints of resistance and possible collapse of the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog...
The Issue: Reports of handle fracture and subsequent disassociation of cam assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Recalled by...
The Issue: Single needle packs in each case ( 10 needles per case) are mislabeled on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HealthTronics Endocare 3.8mm RenalCryo Cryoprobe Recalled by Healthtronics,...
The Issue: The Endocare 3.8mm RenalCryo Cryoprobe is being recalled because the label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.