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. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22401–22420 of 29,188 recalls
Recalled Item: Synthes Application Instrument for Sternal ZIPFIX Recalled by Synthes (USA)...
The Issue: The end cap may loosen and detach making the instrument non-functional. No...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft...
The Issue: Biomet has initiated a recall on Biomet Spine Lineum OCC Starter Flexible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER LH Series Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to Channel Error...
The Issue: Channel Error code is displayed on the PC unit with an audio and visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Kinetics Recalled by Neuro Kinetics, Inc. Due to The devices that...
The Issue: The devices that included the OVAR research test were not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and...
The Issue: The cutting efficiency of the Countersinks was out of specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE Recalled by...
The Issue: Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 2 Waste Management System Docking Station (120V and 230V) Recalled...
The Issue: The Fluid Coupling Sleeve, a component within the Neptune Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0/4.0 Cannulated Drill Bit Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concave Reamer Head Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the Concave and Convex Reamer Heads may be too small to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lightspeed 16 CT Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery ST 16 Recalled by GE Healthcare Due to Potential for expulsion...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery LS Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wall Chart for STERRAD 100NX System Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO Disk Recalled by Microbiologics Inc Due to LYFO Disk Catalog #0983L is...
The Issue: LYFO Disk Catalog #0983L is to contain Candida tropicalis. However, lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking...
The Issue: The locking pin on the RIO Base Array is damaged during assembly onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.