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. 2,603 recalls have been distributed to Tennessee in the last 12 months.
Showing 17001–17020 of 29,188 recalls
Recalled Item: bioMerieux VITEK 2 Gram Positive Cefoxitin Screen Recalled by bioMerieux,...
The Issue: Customer reports indicated an increase in the rate of non-detected MRSA in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Horizon - PET/CT Recalled by Siemens Medical Solutions USA, Inc....
The Issue: Error introduced into PET images acquired and reconstructed with VJ20A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ray Station 4.9 Ray Station 5 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Software issue with Center Beam in Field functionality. Issue can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...
The Issue: The mounts on the monitor may have an insufficient (missing or incomplete) weld.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...
The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Programming System Recalled by LivaNova USA Inc Due to...
The Issue: Unintended warning message displayed on generators programmed with a Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...
The Issue: The recalling firm identified a software issue related to the Patient Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is Recalled by Biomerieux...
The Issue: Missing desiccant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo XT Suture Anchor Recalled by Valeris Medical, LLC Due to The label on...
The Issue: The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8...
The Issue: This Correction is being initiated based on a customer complaint received on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris MCK Onlay Insert Extractor. Recalled by Mako Surgical Corporation...
The Issue: Possible hinge pin disassociation from the Mako Onlay Insert Extractor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoMate 2550 "High Speed" Catalog Number ODL25255 Recalled by Beckman...
The Issue: A misaligned pipette tip sensor poses the remote risk of cross-contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...
The Issue: Potential breakage of the endoscope s insertion tube bending section during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...
The Issue: Breakage of the endoscope's insertion tube bending section during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...
The Issue: Breakage of the endoscope's insertion tube bending section during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...
The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.