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.

52,000 total recalls
2,661 in last 12 months

Showing 1182111840 of 29,188 recalls

Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: Lack of pouch seal. Product is labelled as sterile.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Mediana Co., Ltd.

Recalled Item: DIRECT SUPPLY Attendant VITAL SIGNS MONITOR Recalled by Mediana Co., Ltd....

The Issue: Failures were found in the temperature measurement function while in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) CentraLink Data Management System software version 16.0.2 Siemens...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics Inc.

Recalled Item: Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer...

The Issue: Flexible tubing connected to the liquid waste bottle can crack during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) Atellica Data Manager software version 1.0 Siemens Material Number...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics Inc.

Recalled Item: Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Recalled...

The Issue: Flexible tubing connected to the liquid waste bottle can crack during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Neocis Inc.

Recalled Item: DRW-0739-02: Gen 2 Posterior Chairside Splint LRUL (lower right-upper left)...

The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Neocis Inc.

Recalled Item: DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right)...

The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Neocis Inc.

Recalled Item: DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right)...

The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Bound Tree Medical

Recalled Item: Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Recalled by...

The Issue: Kit contained an incorrect catheter-tip syringe not compatible with the luer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 3.2MM...

The Issue: Distributed to the field without having completed design history files or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. T15 Multi-Directional Locking Screw 3.5mm x 60mm Recalled by Biomet...

The Issue: Distributed to the field without having completed design history files or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 60MM Recalled by...

The Issue: Distributed to the field without having completed design history files or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE...

The Issue: Distributed to the field without having completed design history files or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 14 HOLE 234MM...

The Issue: Distributed to the field without having completed design history files or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 11 HOLE 190MM...

The Issue: Distributed to the field without having completed design history files or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM CALIBRATED DRILL BIT Recalled...

The Issue: Distributed to the field without having completed design history files or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing