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. 2,414 recalls have been distributed to Tennessee in the last 12 months.
Showing 1361–1380 of 52,000 recalls
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The failure occurs if a user on the Omnipod 5 Recalled by Insulet...
The Issue: The failure occurs if a user on the Omnipod 5 iOS application selects and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET...
The Issue: Undeclared allergens (milk).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS...
The Issue: Undeclared allergens (cashews).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline Adult Anesthesia Set Recalled by Medline Industries, LP Due to...
The Issue: Specific items and lots of Medline Kits may contain Clearlink IV Sets which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juggerknot Mini Soft Anchors Recalled by Biomet, Inc. Due to The outer...
The Issue: The outer carton box label is for the JuggerKnot 1.0mm Mini products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to The...
The Issue: The unexpected internal fault / system diagnostic error to result when a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version Recalled by...
The Issue: Potential that the measured value may be smaller than the actual area.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to...
The Issue: Fluctuations may be more likely to occur if the total flow through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Clave Bag Spike w/ChemoLock Port Recalled by ICU Medical, Inc....
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Port Recalled by ICU Medical, Inc. Due to Port weld of...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Bag Spike Recalled by ICU Medical, Inc. Due to Port...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 21" Ext Set w/ChemoLock Port Recalled by ICU Medical, Inc. Due...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 6.5" Bag Spike w/ChemoLock Port Additive Port Recalled by ICU...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Oncology Transfer Kit w/ChemoClave and ChemoLock Port Recalled...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.