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. 2,661 recalls have been distributed to Tennessee in the last 12 months.
Showing 11861–11880 of 29,188 recalls
Recalled Item: ABL80-FLEX CO-OX 393-841 Box Label Recalled by Radiometer Medical ApS Due to...
The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...
The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product Performance Verifier I Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product Performance Verifier II Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...
The Issue: The product is being recalled due to the central screw drill seizing inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...
The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...
The Issue: An error in the calculation of the Michigan Ranges can generate an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Compression Screw Recalled by Stryker GmbH Due to Seal integrity of...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S Recalled by...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If an examination is interrupted when the InSpect Projection View (PV) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1 End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.