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. 2,568 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,568 in last 12 months

Showing 661680 of 48,326 recalls

Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: FORCEP Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...

The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...

The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...

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

Class II — Potential Health HazardOngoing
DrugNovember 12, 2025· Medical Products Laboratories, Inc.

Recalled Item: Walgreens Saline Nasal Spray WITH XYLITOL Recalled by Medical Products...

The Issue: Microbial contamination of a non-sterile product - microorganism found to be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 12, 2025· Howmedica Osteonics Corp.

Recalled Item: The Stryker CranialMask Tracker is a single-use device consisting of...

The Issue: When the device is activated during surgery, the device software issues an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2025· Cardinal Health 200, LLC

Recalled Item: ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full...

The Issue: Affected gowns have the incorrect expiration date on the product packaging....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2025· Remel, Inc

Recalled Item: 1. CAMHB W/LHB Recalled by Remel, Inc Due to Products may contain...

The Issue: Products may contain contamination, which may result in a darker or brown...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
FoodNovember 11, 2025· Lexunder Inc

Recalled Item: Food to Live brand ORGANIC SUPERGREENS POWDER MIX Recalled by Lexunder Inc...

The Issue: Contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2025· Lexunder Inc

Recalled Item: Food to Live brand ORGANIC MORINGA LEAF POWDER Recalled by Lexunder Inc Due...

The Issue: Contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing