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. 2,526 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,526 in last 12 months

Showing 96619680 of 48,326 recalls

DrugFebruary 15, 2023· AVEVA Drug Delivery Systems, Inc.

Recalled Item: Buprenorphine Transdermal System Recalled by AVEVA Drug Delivery Systems,...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2023· AVEVA Drug Delivery Systems, Inc.

Recalled Item: Buprenorphine Transdermal System Recalled by AVEVA Drug Delivery Systems,...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2023· RISING PHARMACEUTICALS

Recalled Item: Warfarin Sodium Tablets Recalled by RISING PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2023· Foundation Medicine, Inc.

Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...

The Issue: An incorrect negative claim was identified on the claims page; the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· Merit Medical Systems, Inc.

Recalled Item: Flex-Neck Catheter External Repair Kit LOT CE-1400/A Recalled by Merit...

The Issue: Product that was built for design verification testing was inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM Recalled by...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2023· Nanomaterials Discovery Corporation

Recalled Item: Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer...

The Issue: Chemical Contamination: FDA analysis found the product to contain methanol,...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 14, 2023· Pharmedica USA, LLC

Recalled Item: Purely Soothing 15% MSM Drops Recalled by Pharmedica USA, LLC Due to...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 14, 2023· Pharmedica USA, LLC

Recalled Item: Purely Soothing MSM Nasal Spray Recalled by Pharmedica USA, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 14, 2023· Wismettac Asian Foods, Inc.

Recalled Item: Chili Pepper Powder (ICHIMI TOGARASHI) 300g Brand: Shirakiku Recalled by...

The Issue: Product was found to contain sesame that were not declared on the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 14, 2023· Wismettac Asian Foods, Inc.

Recalled Item: SPICE SHICHIMI TOGARASHI 300g Brand: Shirakiku Distributed by: Recalled by...

The Issue: Product was found to contain sesame that were not declared on the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES AUX Tower BD Pyxis Recalled by CareFusion 303, Inc....

The Issue: Due to an increase in complaints of door latch assembly failures that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2023· Pro-Dex Inc

Recalled Item: KLS martin Group KLS E-COUPLING ADAPTER E-Coupling Adapter Recalled by...

The Issue: Incorrect Unique Device Identifier/GTIN code was used on product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2023· Edwards Lifesciences, LLC

Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...

The Issue: There is a potential that the distal end of the catheter may be bent beyond...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2023· Edwards Lifesciences, LLC

Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...

The Issue: There is a potential that the distal end of the catheter may be bent beyond...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2023· Defibtech, LLC

Recalled Item: DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on...

The Issue: A component of a sub-assembly used in the affected AEDs had not undergone...

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

Class II — Potential Health HazardOngoing