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. 2,638 recalls have been distributed to Tennessee in the last 12 months.
Showing 13441–13460 of 29,188 recalls
Recalled Item: STRATAFIX Spiral PDS Plus Violet 18 (45cm) CT-1 Needle Product Recalled by...
The Issue: The product does not meet certain internal strength testing specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...
The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....
The Issue: FDA inspection identified that due to increased positivity (false positives)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian Multileaf Collimator [MLC] Recalled by Varian Medical Systems, Inc....
The Issue: After a recent upgrade to the collimator software version 8.5, the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Nexframe Stereotactic System and StealthStation Cranial software...
The Issue: Entry point and lead placement inaccuracies during deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Abutment Engaging CC RP pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Base CC RP 1.5 mm Recalled by Nobel Biocare Usa Llc Due to...
The Issue: Packages of abutments (universal base) may contain an incorrect screw. While...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Snap Abutment Engaging CC RP 1.5 mm Recalled by Nobel Biocare Usa...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Snappy Abutment 5.5 CC RP 3 mm Recalled by Nobel Biocare Usa Llc Due to...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN:...
The Issue: The assigned value for Rheumatoid Factor over recovers against the material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN:...
The Issue: The assigned value for Rheumatoid Factor over recovers against the material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus XR/a (SlOK : K993090) Recalled by GE Healthcare, LLC Due to...
The Issue: Intermittently not receiving an audible exposure indication upon completion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline SYRINGE Recalled by Medline Industries Inc Due to Samples in the...
The Issue: Samples in the identified lot were found to have incomplete or open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE basic sytem Recalled by Radiometer Medical ApS Due to The firm has...
The Issue: The firm has become aware that there is a potential problem relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.