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. 2,548 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,548 in last 12 months

Showing 49815000 of 48,326 recalls

DrugJune 26, 2024· Guru Inc.

Recalled Item: Infla-650 Herbal Dietary Supplement Recalled by Guru Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found product to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Medisca Inc.

Recalled Item: Budesonide Recalled by Medisca Inc. Due to CGMP Deviations and Presence of...

The Issue: CGMP Deviations and Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sevelamer Carbonate for Oral Suspension 0.8g packets Recalled by Dr. Reddy's...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2024· RemedyRepack Inc.

Recalled Item: Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules Recalled...

The Issue: CGMP Deviations: Out of specification for dissolution

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· Amerisource Health Services LLC

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 25, 2024· UNIMAX MEDICAL SYSTEMS INC

Recalled Item: 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch Recalled by...

The Issue: The tube may fall into the surgical site during the grasping process.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2024· Preat Corp

Recalled Item: Multiple Digital Analog Products labeled as: NobelBiocare...

The Issue: Due to a manufacturing issue, the product has a out of specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FH Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FM Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK MINI CR-4HH-P Recalled by CareFusion 303, Inc. Due to Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing