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 27941–27960 of 29,188 recalls
Recalled Item: Siemens syngo WorkFlow SLR Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Under certain conditions, when using the Search functionality, the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 VCC P/N 4598 001 41341 REV A Recalled by Philips Medical Systems...
The Issue: Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSX PROXIMATE Skin Staple Extractor Recalled by Ethicon Endo-Surgery Inc Due...
The Issue: Damage to the packaging may have compromised the sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranawat/Burnstein Acetabular Shell 54mm/Limited Holes/Porous Coated is a...
The Issue: The color code on label conflicts with the liner size (liner size 24 should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) product Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling all lots of Sterrad...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: West Nile Virus IgG DxSelect" kit Catalog No. EL0300G Kit Lots 122150...
The Issue: The firm recalled due to higher reactivity with some samples in the effected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Repeater Pump Recalled by Baxa Corporation Due to The firm is issuing a...
The Issue: The firm is issuing a field correction to the operators manual included with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD Recalled...
The Issue: BD received a complaint report for mixed syringe tips (oral and non-oral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardio Imaging 5.0 is a software only Picture Archiving Recalled...
The Issue: GE Healthcare is aware of a potential safety risk where an image labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178...
The Issue: Broken screw insertor hardness was measured and found to be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical, Inc. has identified a potential comingling of components where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...
The Issue: Potential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical System Extended Brilliance Workspace (EBW) Recalled by...
The Issue: Incorrect values may be displayed. Philips is issuing a software update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Philips Medical Systems...
The Issue: Philips is issued a Field Change Order to update Extended Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...
The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) BenchMark ULTRA Recalled by Ventana...
The Issue: Potiential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...
The Issue: The insert provided with the product for the specific lot number indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...
The Issue: A product complaint was received where a size 20 screw was labeled as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.