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 16461–16480 of 29,188 recalls
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX PST01199 BARIATRIC TRISTAPLE (Item Number: PST01199) (2) BOX PST03403...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX KITDE0183 APPENDIX LIPPE DETMOLD (KITDE0183) (2) KIT-DE-0083...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.