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. 2,636 recalls have been distributed to Tennessee in the last 12 months.
Showing 15601–15620 of 29,188 recalls
Recalled Item: Bronchovideoscope BF-3C40 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-MP160F Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-P180 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-P40 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic Bronchoscope BF-UC180F Recalled by Olympus Corporation of the...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-MP60 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-1T180 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-40 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-1T40 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovidescope BF-1T240 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-P160 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-3C160 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite 23 GA Vit Cutter Recalled by Bausch & Lomb Inc...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite 20 GA Vit Cutter Recalled by Bausch & Lomb Inc...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.