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. 2,710 recalls have been distributed to Tennessee in the last 12 months.
Showing 2521–2540 of 29,188 recalls
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...
The Issue: Potential for procedural delays or interruptions during use of the Auryon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver with Software Recalled by Spacelabs Healthcare,...
The Issue: Telemetry receivers with affected software versions may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse PRO The Spacelabs model 98700 is a Recalled by Spacelabs Healthcare,...
The Issue: Due to a manufacturing error the incorrect device serial number was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Mini The Eclipse MINI Model 98900 is Recalled by Spacelabs...
The Issue: Due to a manufacturing error the incorrect device serial number was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code Recalled...
The Issue: Due to complaints received for the marker band detaching from the distal tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - Donaldson - Blue Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - Donaldson - Double - Blue Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.