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 4046140480 of 48,326 recalls

Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2014· Qualitest Pharmaceuticals

Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...

The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2014· Qualitest Pharmaceuticals

Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...

The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2014· Qualitest Pharmaceuticals

Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...

The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2014· Akorn, Inc.

Recalled Item: Rifampin for Injection USP Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurity/Degradation Specification; high out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: ZyGenerics ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Superpotent Drug: A complaint was reported by a pharmacist who stated...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 5, 2014· ICU Medical, Inc.

Recalled Item: Port Access Kit with MicroClave Clear Connector Recalled by ICU Medical,...

The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· ICU Medical, Inc.

Recalled Item: CAP Change Kit w/MicroClave Clear Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· Curbell Medical, Inc.

Recalled Item: CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor...

The Issue: The firm became aware of a potential problem that was initiated by a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· ICU Medical, Inc.

Recalled Item: Cap Change Kit with MicroClave Clear Connector Recalled by ICU Medical, Inc....

The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2014· Medical Components, Inc dba MedComp

Recalled Item: Split Cath III Trays Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2014· Baxter Healthcare Corp

Recalled Item: ProSol - sulfite-free (Amino Acid) Injection Recalled by Baxter Healthcare...

The Issue: Presence of Particulate Matter: identification of particulates in a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2014· Cubist Pharmaceuticals, Inc.

Recalled Item: CUBICIN (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter: Potential presence of glass particulate...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 1, 2014· Ortho Molecular Products Inc

Recalled Item: Ortho Molecular Products LifeCORE Recalled by Ortho Molecular Products Inc...

The Issue: Ortho Molecular Products is recalling all lots of LifeCore Chocolate and...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 1, 2014· Ortho Molecular Products Inc

Recalled Item: Ortho Molecular Products LifeCORE Complete Recalled by Ortho Molecular...

The Issue: Ortho Molecular Products is recalling all lots of LifeCore Chocolate and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 1, 2014· Sorin Group USA, Inc.

Recalled Item: ST¿CKERT HeaterCooler System 3T Recalled by Sorin Group USA, Inc. Due to On...

The Issue: On August 1, 2014 Sorin Group USA, Inc. informed consignees via letter to...

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

Class II — Potential Health HazardOngoing
DrugJuly 31, 2014· Ben Venue Laboratories Inc

Recalled Item: CYTARAbine for Injection USP Recalled by Ben Venue Laboratories Inc Due to...

The Issue: Lack of Assurance of Sterility: Crimp defects during visual inspection could...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 31, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray V21 Recalled by Mindray DS USA, Inc. dba Mindray North America Due...

The Issue: Mindray DS USA Inc. initiated a voluntary field corrective action for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Carefusion 2200 Inc

Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...

The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Roche cobas IT 1000 Product Usage: Intended Use: An electronic Recalled by...

The Issue: Potential that test results would be assigned to the wrong Patient ID if...

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

Class II — Potential Health HazardOngoing