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. 941 recalls have been distributed to Tennessee in the last 12 months.
Showing 45961–45980 of 52,000 recalls
Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...
The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR (various sizes) Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 COCR FEMORAL HEAD (2 Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 X 10 CORT SCREW SELFT 3.5 X 12 CORT Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRESSFIT FEM ST FX 16 X 1 Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 X 6 CORT SCREW HEX/SE 2.0 X 6 CORT Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...
The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA Recalled by Zimmer, Inc....
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM HD ION (various sizes) Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.