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. 2,340 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,340 in last 12 months

Showing 3566135680 of 48,326 recalls

Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
FoodAugust 31, 2015· The Ice Cream Club, Inc.

Recalled Item: Caramel Caribou Ice Cream Recalled by The Ice Cream Club, Inc. Due to...

The Issue: Product contains undeclared peanuts

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 28, 2015· VRVK Nutraceuticals, LLC

Recalled Item: DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT...

The Issue: The dietary supplement contains undeclared milk and crustacean shellfish...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 27, 2015· Nutraceutical International Corporation

Recalled Item: KAL Brand Amino Acid Complex Recalled by Nutraceutical International...

The Issue: Undeclared allergen, casein is a disclosed ingredient, but the word milk not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 27, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...

The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.

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

Class III — Low RiskOngoing
Medical DeviceAugust 27, 2015· Arrow International Inc

Recalled Item: Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes...

The Issue: Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2015· Zimmer, Inc.

Recalled Item: Zimmer Guide Wires for orthopedic procedures. Recalled by Zimmer, Inc. Due...

The Issue: Product labeling of these sterile guide wires (external carton label and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2015· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Multianalyte Controls Recalled by Alere San Diego, Inc....

The Issue: Alere San Diego is recalling the Alere Cholestech LDX Multianalyte Control...

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

Class III — Low RiskOngoing
DrugAugust 27, 2015· The One Minute Miracle Inc

Recalled Item: MIRACLE DIET 30 capsules Recalled by The One Minute Miracle Inc Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 27, 2015· The One Minute Miracle Inc

Recalled Item: MIRACLE ROCK 48 capsules Recalled by The One Minute Miracle Inc Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 27, 2015· Becton Dickinson & Co.

Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...

The Issue: BD has confirmed that a portion of tests associated with the affected lots(...

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

Class II — Potential Health HazardOngoing
FoodAugust 26, 2015· General Mills, Inc

Recalled Item: Cascadian Farm Organic Cut Green Beans Recalled by General Mills, Inc Due to...

The Issue: General Mills is recall one lot of 10 ounce bags of frozen Cascadian Farm...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 26, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo Lab Data Manager System - Product Usage: syngo Lab Recalled by Siemens...

The Issue: Software Issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2015· Edwards Lifesciences, LLC

Recalled Item: ThruPort Knot Pusher. This device is sold individually (Model KP1) Recalled...

The Issue: The configuration of the slot at the tip of the knot pusher may inhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to...

The Issue: Cross-threading of the hemostasis valve may occur if it is tightened with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to...

The Issue: Cross-threading of the hemostasis valve may occur if it is tightened with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2015· Cardinal Health

Recalled Item: Ambitex NMD400 Nitrile Exam Gloves size medium. General Hospital and...

The Issue: Ambitex Nitrile NMD400 Exam Gloves size medium on exam hold were...

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

Class II — Potential Health HazardOngoing
DrugAugust 25, 2015· Hospira, Inc.

Recalled Item: 1% Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: particulate matter identified as iron oxide,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2015· Apotex Inc.

Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Black Widow 25 Ephedra Super Potent Fat Burner Dietary Supplement Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund