Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,568 recalls have been distributed to Montana in the last 12 months.
Showing 1301–1320 of 48,326 recalls
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: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180 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-H1100 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 b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 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: TENACIO Pump with InhibiZone Recalled by Boston Scientific Corporation Due...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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 II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 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: 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-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: 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 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: Goot Essa Recalled by GOOT ESSA, LLC Due to Potential Listeria Contamination
The Issue: The firm had a positive Listeria Monocytogenes on a sample from this batch...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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: 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: ICU Medical ChemoLock Vial 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 30" (76 cm) Appx 3.3 mL Recalled by ICU Medical, Inc. Due to...
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 Graduated Connector w/ChemoLock Port Recalled by ICU Medical,...
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 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.