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. 1,056 recalls have been distributed to Tennessee in the last 12 months.
Showing 16621–16640 of 52,000 recalls
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Captia Measles IgM Kit Recalled by Clark Laboratories, Inc....
The Issue: Positive Control may run high out of its assigned ISR range and result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #:...
The Issue: Discrepancy in labeling between the adult CBC ranges presented in the OLO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...
The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...
The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...
The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Telmisartan Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label-mixup
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port Recalled by...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Controller - Product Usage: intended for use with a Recalled by Boston...
The Issue: May have been programmed with a less than optimal brightness setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Abre Venous Self-expanding Sent System Recalled by Medtronic Inc....
The Issue: Incorrect size printed on the device; packaging is labeled correctly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...
The Issue: bioMerieux received complaints about calibration issue observed on several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Admin Set w/ClaveTM Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros Closed Male Luer - Product Usage: provides Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 45" (114 cm) Appx 1.7 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Appx 0.50 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.