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. 2,306 recalls have been distributed to Montana in the last 12 months.
Showing 41901–41920 of 48,326 recalls
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...
The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...
The Issue: Incorrect master label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...
The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...
The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...
The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alprazolam Extended-Release Tablets Recalled by Actavis Elizabeth LLC Due to...
The Issue: Failed Dissolution Specifications: Product did not meet specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan...
The Issue: Presence of Precipitate: Recall is due to complaints of a white substance,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candy coated popcorn shaped into a heart weighing 1.5 ounces Recalled by...
The Issue: The Nutrition Facts and allergen label was not applied individual popcorn...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Simplexa Flu AlB & RSV Direct Assay Kits Recalled by Focus Diagnostics Inc...
The Issue: Focus Diagnostics initiated the recall of the certain Simplexa Flu AlB & RSV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...
The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F180NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200A High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.