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. 2,284 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,284 in last 12 months

Showing 4380143820 of 48,326 recalls

DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Silver Sword capsules Recalled by Fabscout Entertainment, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Clalis capsules Recalled by Fabscout Entertainment, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Hospira Inc.

Recalled Item: Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer report of visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2013· Insight Instruments, Inc.

Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...

The Issue: The product was registered and distributed as a Class I medical device and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Mar Cor Purification

Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...

The Issue: High inlet water pressure beyond specification and the solenoid valve does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...

The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...

The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS zee and zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens issued a customer safety advisory notice and field safety corrective...

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

Class II — Potential Health HazardOngoing
DrugJune 25, 2013· Apotex Inc

Recalled Item: Latanoprost Ophthalmic Solution Recalled by Apotex Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: Failed at expiry for Preservative...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 25, 2013· Talenti Gelato

Recalled Item: Talenti Gelato Recalled by Talenti Gelato Due to Undeclared Allergen

The Issue: Product contains undeclared Allergen; Pecans.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533)...

The Issue: ADVIA Centaur Homocysteine dilution recovery on the diluent identified the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL + Recalled by Convatec Inc. Due to ConvaTec...

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL Fecal Management System Recalled by Convatec Inc....

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
DrugJune 24, 2013· Fresenius Kabi USA, LLC

Recalled Item: Oxytocin Injection Recalled by Fresenius Kabi USA, LLC Due to Subpotent...

The Issue: Subpotent Drug; 15-month stability test station

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2013· Stelkast Co

Recalled Item: SC2316 Recalled by Stelkast Co Due to The firm became aware of an incident...

The Issue: The firm became aware of an incident relating to a breach of sterility in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-852-000 (Console 230V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing