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. 2,277 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,277 in last 12 months

Showing 4462144640 of 48,326 recalls

DrugMay 20, 2013· Hospira, Inc.

Recalled Item: Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate; lot being recalled as a precaution due to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 20, 2013· Sandoz Incorporated

Recalled Item: Methotrexate Injection Recalled by Sandoz Incorporated Due to Presence of...

The Issue: Presence of Particulate Matter: Found during examination of retention samples.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 20, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...

The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2013· Olympus America Inc.

Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...

The Issue: There is a possibility that the pump head was not shipped in the locked...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2013· Steris Corporation

Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...

The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...

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

Class II — Potential Health HazardOngoing
DrugMay 17, 2013· Warner Chilcott US LLC

Recalled Item: Enablex (darifenacin) Extended Release Tablet Recalled by Warner Chilcott US...

The Issue: Failed Impurities/Degradation Specifications: unspecified degradation product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 17, 2013· SpineFrontier, Inc.

Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...

The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· RF Technologies, Inc.

Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....

The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...

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

Class II — Potential Health HazardOngoing
DrugMay 16, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...

The Issue: Presence of Foreign Substance: Belladonna Alkaloids with Phenobarbital...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...

The Issue: Cross contamination with other products: Belladonna Alkaloids with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2013· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Solbar Q Soy Protein Isolates. Item No. / Item Description: Recalled by Chs...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Contex - Textured Soy Protein Concentrates Item No. / Item Recalled by Chs...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Solcon Soy Protein Concentrates. Item No. / Item Description: 12110 Recalled...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Solcon S Functional Soy Protein Concentrates. Item No. / Item Recalled by...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2013· The Standing Company

Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...

The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing