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. 2,359 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,359 in last 12 months

Showing 2826128280 of 48,326 recalls

FoodJune 9, 2017· High Liner Foods Inc.

Recalled Item: HFS 1/10 Oven Ready Breaded Calamari Strips 0.50 oz. avg. Item Number:...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 9, 2017· High Liner Foods Inc.

Recalled Item: HFS 1/10.35 Oven Ready Krispy Krunchy Breaded Alaska Pollock Fillets 3.6 oz....

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 9, 2017· High Liner Foods Inc.

Recalled Item: American Pride 1/10lb Fully Cooked Gourmet Breaded Pollock Squares 2 oz....

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 9, 2017· High Liner Foods Inc.

Recalled Item: HLSC 1/10lb Honey Chipotle Salmon Recalled by High Liner Foods Inc. Due to...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 9, 2017· High Liner Foods Inc.

Recalled Item: HFS 1/40 Crunchy Breaded Ocean Perch Fillet 2-3oz WIP. Item Number: 19905610...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 9, 2017· Sorin Group USA, Inc.

Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...

The Issue: Identification of excess plastic on the tip of the cannula.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Penumbra Inc.

Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...

The Issue: Penumbra has identified an issue in these four lots involving a raw material...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
DrugJune 8, 2017· Phillips Co.

Recalled Item: TetraStem brand Topical Ointment First Aid Antibiotic Recalled by Phillips...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: StaphWash+Plus+ Skin Protectant Recalled by Phillips Co. Due to GMP...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: VenomX Recalled by Phillips Co. Due to GMP Deviations; FDA inspection found...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume) Recalled...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: Tetracycline-ABC Brand Topical ointment First Aid Antibiotic Recalled by...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: Diabecline brand Topical Ointment First Aid Antibiotic Recalled by Phillips...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 8, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...

The Issue: Certain iOS and Android App versions contain a program error (bug) in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect diabetes management software app Recalled by Roche...

The Issue: Certain iOS and Android App versions contain a program error (bug) in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing