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. 1,101 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,101 in last 12 months

Showing 1441–1460 of 48,326 recalls

Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM Solution Set Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
FoodAugust 29, 2025· ROLLING PIN BAKING COMPANY LLC

Recalled Item: Rolling Pin brand Dubai Style Chocolate Recalled by ROLLING PIN BAKING...

The Issue: Product does not declare wheat in the allergen statement.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2025· ImaCor Inc.

Recalled Item: ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound...

The Issue: Production assembly error resulting in the potential for reversed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX...

The Issue: To provide further information to the user to ensure proper use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model...

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2025· Fagron Compounding Services

Recalled Item: bevacizumab (Avastin) Injection Recalled by Fagron Compounding Services Due...

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
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model...

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter....

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Solution Set Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Getinge Disinfection Ab

Recalled Item: Getinge 88-Series Washer- Disinfector. Model Number: 88-5. Recalled by...

The Issue: Potential for device to overheat during operation if the circulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model...

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Paclitaxel Set Recalled by Baxter Healthcare Corporation...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing