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. 2,400 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,400 in last 12 months

Showing 2110121120 of 48,326 recalls

DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On Recalled by...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 21, 2019· Alto Development Corp

Recalled Item: A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire...

The Issue: Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets 50 mg 1000 Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2019· Perrigo Company PLC

Recalled Item: Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron...

The Issue: Product may contain metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: HYDROXOCOBALAMIN 1000 MCG/ML (MDV) Recalled by RXQ Compounding LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: KETAMINE 10 MG/ML INJ SOL SYR (C-III) Recalled by RXQ Compounding LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: TURBO CAINE 2.5 (PHEN2.5/CYCLO1/ TROP1/TETRA 0.5) Recalled by RXQ...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: GLUTATHIONE 200MG/ML (MDV) INJECTION SOLN Recalled by RXQ Compounding LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: VITAMIN B COMPLEX 100 (MDV) Recalled by RXQ Compounding LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund