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. 2,322 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,322 in last 12 months

Showing 3770137720 of 48,326 recalls

FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: Deluxe Mixed Nuts with Sea Salt: Aurora Recalled by Aurora Products, Inc....

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: Raisin Nut Party Mix: Aurora Recalled by Aurora Products, Inc. Due to...

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· La Terra Fina, Inc.

Recalled Item: La Terra Fina Organic Thick & Creamy Spinach Dip and Spread Recalled by La...

The Issue: Firm was notified by their supplier of IQF chopped spinach that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: Deluxe Mixed Nuts No Salt: Aurora Recalled by Aurora Products, Inc. Due to...

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: 5 K Omega Trail Mix: Aurora 20 oz. Plastic Cup Recalled by Aurora Products,...

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· La Terra Fina, Inc.

Recalled Item: La Terra Fina Chunky Spinach Artichoke & Parmesan Dip 31-ounce Recalled by...

The Issue: Firm was notified by their supplier of IQF chopped spinach that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: Roasted Salt Mixed Nuts: Aurora Recalled by Aurora Products, Inc. Due to...

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· La Terra Fina, Inc.

Recalled Item: La Terra Fina Spinach Artichoke & Parmesan Dip made with Recalled by La...

The Issue: Firm was notified by their supplier of IQF chopped spinach that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: 6 Section Nut Tray Assortment: Aurora Recalled by Aurora Products, Inc. Due...

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: Walnuts: America Choice Recalled by Aurora Products, Inc. Due to Potential...

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 19, 2015· Biosense Webster, Inc.

Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...

The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2015· Biomet, Inc.

Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...

The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2015· Mylan Institutional LLC

Recalled Item: CARBOplatin Injection 450 mg/45 mL (10 mg/mL) Recalled by Mylan...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 18, 2015· Mylan Institutional LLC

Recalled Item: Methotrexate Injection Recalled by Mylan Institutional LLC Due to Presence...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 18, 2015· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2015· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2015· Bard Peripheral Vascular Inc

Recalled Item: Bard Monopty Disposable Core Biopsy Instruments and Kits Recalled by Bard...

The Issue: Bard Peripheral Vascular is recalling the Bard Monopty Disposable Core...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Dual Chamber Temporary External Pacemaker Recalled by Medtronic...

The Issue: Possible performance issue when used with specific AA-sized (LR6) batteries....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Biocare Medical, LLC

Recalled Item: CD99 Catalog number PM008 AA Recalled by Biocare Medical, LLC Due to A drop...

The Issue: A drop in staining intensity over time has been observed. These lots may not...

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

Class II — Potential Health HazardOngoing