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. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22121–22140 of 29,188 recalls
Recalled Item: Synthes Threaded Plate Holder- Long for 3.5mm Locking Hold Recalled by...
The Issue: The affected part number and lot listed above is incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helioseal F Sealant 1 x 1.25 g Recalled by Ivoclar A. G. Due to A defect...
The Issue: A defect occurred in the production process of Helioseal F Sealant; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed Recalled by...
The Issue: Hill-Rom is voluntarily recalling the Hill-Rom 100 Low Bed due to complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry XPT Systems Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Multiple Software issues. Auto Start-UP Fail, Calibration Interval Resets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.7 mm Locking Screw SLF-TPNG with T8 Stardrive Recess 12mm. Recalled by...
The Issue: Specific lots of the SS 2.7mm locking screw have been mislabeled as SS 2.4mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn KleenSpec Corded Illumination System Recalled by Welch Allyn Inc...
The Issue: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Antibacterial Hydro Personal Catheter Recalled by C.R. Bard, Inc. Due to...
The Issue: Incorrect unit labeling. The case label and shelf box are correct, Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The "Pacifier Activated Lullaby" (PAL) System composed of three major...
The Issue: PAL unit has undergone significant technological changes since the previous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...
The Issue: Reporting feature times out after inactivity for more than an hour sending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...
The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump Recalled by...
The Issue: The device might fail to detect air in line while infusing the medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...
The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Erroneous low results on a small number of reagent wells. There is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...
The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Achieve Cables Recalled by Medtronic Inc. Due to 64 units of...
The Issue: 64 units of Achieve Electrical Cables were shipped with a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...
The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm-...
The Issue: The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.