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. 2,400 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,400 in last 12 months

Showing 2250122520 of 48,326 recalls

Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: Urodiagnost Recalled by Philips North America, LLC Due to The locking plate...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: URODiagnost Eleva Recalled by Philips North America, LLC Due to The locking...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: Omnidiagnost Classic Recalled by Philips North America, LLC Due to The...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: MultiDiagnost-Eleva Recalled by Philips North America, LLC Due to The...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Small Diameter Cement Plug Inserter-Sterile Recalled by Zimmer...

The Issue: Lack of an adequate sterilization validation

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Becton Dickinson & Company

Recalled Item: SmartSite Syringe Administration Set-Product Package Size 50 Recalled by...

The Issue: Leaking of the Smartsite Syringe Administration Set. May result in delay or...

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

Class I — Serious Health HazardOngoing
FoodFebruary 28, 2019· Fungi Perfecti LLC

Recalled Item: Host Defense MycoBotanicals Blood Sugar Recalled by Fungi Perfecti LLC Due...

The Issue: Host Defense MycoBotanicals Blood Sugar, 60 ct. bottles, is recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Camber Pharmaceuticals Inc

Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Camber Pharmaceuticals Inc

Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Camber Pharmaceuticals Inc

Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2019· Brainlab AG

Recalled Item: Spine & Trauma 3D Navigation 1.0 (subpart of the system Recalled by Brainlab...

The Issue: In certain occurrences, the affected navigation software application might...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 26, 2019· Biomet 3i, LLC

Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...

The Issue: During manufacturing, the screw stop ledge was not made to specification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Abbott Gmbh & Co. KG

Recalled Item: Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: Recalled by...

The Issue: The safety interlock covering the septum piercing probes within the bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Biomet 3i, LLC

Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...

The Issue: During manufacturing, the screw stop ledge was not made to specification and...

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

Class II — Potential Health HazardOngoing