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. 2,436 recalls have been distributed to Tennessee in the last 12 months.
Showing 461–480 of 52,000 recalls
Recalled Item: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical TID Pharos Illuminated Depressor Recalled by Vortex Surgical...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER...
The Issue: Product contains potentially harmful dosing errors for Vecuronium,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument....
The Issue: Presence of particulates in affected devices that can be deposited into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Recalled by Intuitive Surgical, Inc. Due to Access Port System...
The Issue: Access Port System tray may develop cracks potentially resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10F Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: So Delicious Dairy Free Salted Caramel Cluster Cashewmilk Recalled by...
The Issue: Foreign material
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer...
The Issue: Product contains potentially harmful dosing errors for Vecuronium,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number:...
The Issue: The console label for affected devices is missing the "DANGER" symbol.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrone RIA Recalled by Immunotech A.S. Due to The affected Estrone RIA kit...
The Issue: The affected Estrone RIA kit lots may rarely give falsely high patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Duo Precision IV Pump Recalled by ICU Medical, Inc. Due to...
The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.