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 27781–27800 of 29,188 recalls
Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...
The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...
The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...
The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...
The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo Cardiovascular System (TCVS) has received reports of a situation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...
The Issue: This notice is being provided in follow up to the field correction initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica ASP6025 Vacuum Tissue Processor The Leica ASP6025 is a Recalled by...
The Issue: The Instruction for Use 1v9 and all previous versions specify incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vertex Max Drill Tube is a component within the Recalled by Medtronic...
The Issue: Medtronic is recalling certain Vertex Max Drill Tubes which are used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Spine Ardis Inserter Recalled by Zimmer, Inc. Due to Zimmer Spine has...
The Issue: Zimmer Spine has received reports of the PEEK Ardis Interbody Spacer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes...
The Issue: BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...
The Issue: Greatbatch Medical observed some anomalies of the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.