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. 1,071 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,071 in last 12 months

Showing 6781–6800 of 48,326 recalls

FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Turtle Brownie (12 pieces/cookies)...

The Issue: Undeclared Allergens - Milk and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2023· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tacrolimus Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules: One 0.5 mg Tacrolimus capsule found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Peanut Butter Chocolate Chunk (12...

The Issue: Undeclared Allergens - Milk and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Chocolate Chili Coconut (12...

The Issue: Undeclared Allergens - Milk and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies)...

The Issue: Undeclared Allergens - Milk and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Lemon Sugar Cookie/Lemon Shortbread (12...

The Issue: Undeclared Allergens - Milk and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Brown Butter Honey Pistachio (12...

The Issue: Undeclared Allergens - Milk and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 14, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel Plus (Pneumoplus) Recalled by BioFire Diagnostics,...

The Issue: Their is a potential for false positive results when using Pneumonia panel.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...

The Issue: Their is a potential for false positive results when using Pneumonia panel.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2023· Maquet Cardiovascular, LLC

Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...

The Issue: Express chest drains are pre-packaged with sterile water syringes which have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2023· Diasorin Inc.

Recalled Item: DiaSorin LIAISON HSV-2 Type Specific IgG Recalled by Diasorin Inc. Due to...

The Issue: DiaSorin has identified that lots 136344, 136344A, 136344B, 136344C, 136520,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2023· PHILIPS MEDICAL SYSTEMS

Recalled Item: Spectral CT 7500: Software Version 5.0 Recalled by PHILIPS MEDICAL SYSTEMS...

The Issue: A software issue that can incorrectly label all captured images that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2023· PHILIPS MEDICAL SYSTEMS

Recalled Item: Spectral CT on Rails: Software Version 5.1.0.X Recalled by PHILIPS MEDICAL...

The Issue: A software issue that can incorrectly label all captured images that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2023· Maquet Cardiovascular, LLC

Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...

The Issue: Express chest drains are pre-packaged with sterile water syringes which have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
FoodDecember 13, 2023· WS Global Inc

Recalled Item: Himalayan Pain Relief Tea for Gout and Hangover Recalled by WS Global Inc...

The Issue: Contains undeclared drugs Diclofenac and Dexamethasone Acetate

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2023· GlaxoSmithKline LLC

Recalled Item: ANORO ELLIPTA (umeclidinium and vilanterol inhalation powder) 62.5...

The Issue: Failed Release Testing: Coarse Particle Mass for umeclidinium Out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 12, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion system Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: System may exhibit a loss of imaging functionality and data due to an issue...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2023· Steris Corporation

Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...

The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2023· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate Recalled by Greiner...

The Issue: Tubes have missing additive/anticoagulant resulting in clotting in most...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2023· Steris Corporation

Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...

The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing