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. 2,359 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,359 in last 12 months

Showing 3014130160 of 48,326 recalls

Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF#...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2017· GE Healthcare, LLC

Recalled Item: Table Patient Step on RFX/SFX Recalled by GE Healthcare, LLC Due to Reported...

The Issue: Reported incidents of a patient step detaching from the table. A fall from a...

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

Class II — Potential Health HazardOngoing
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 750 mg added to 250 mL 0.9% Sodium Chloride For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.25 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.5 g added to 0.9% Sodium Chloride 250 Recalled by SCA...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 750 mg added to 5% Dextrose 250 mL For IV Use Only Recalled...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.5 gram added to 5% Dextrose 500 mL Recalled by SCA...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.25 g added to 5% Dextrose 250 mL Bag For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· Amerisource Health Services

Recalled Item: GlipiZIDE Extended-release tablets Recalled by Amerisource Health Services...

The Issue: Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2017· Apotex Inc.

Recalled Item: CycloSPORINE Capsules Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradations Specifications; out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2017· Sandoz Inc

Recalled Item: Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due...

The Issue: Labeling: Incorrect Instructions:outer carton contains the incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2017· Sage Products Inc

Recalled Item: Q Care Continue Care Kit for the non-ventilated patient Recalled by Sage...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2017· Teva Pharmaceuticals USA

Recalled Item: Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class II — Potential Health HazardOngoing
Refund