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. 999 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
999 in last 12 months

Showing 21581–21600 of 48,326 recalls

Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: ECG Trunk Cables: REF/Catalog Number Description 2106305-001 ECG Trunk Cable...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: Replacement ECG leadwires with snap ends REF/Catalog Number Description...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· Cardiocommand Inc.

Recalled Item: CardioCommand Recalled by Cardiocommand Inc. Due to Possible corrosion of...

The Issue: Possible corrosion of the battery contact(s).

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· Cadence Science, Inc.

Recalled Item: Cadence Science Pressure Control Glass Syringe Recalled by Cadence Science,...

The Issue: The glass syringe used with Pressure Control Syringes may potentially break...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2019· I.T.S. GmbH

Recalled Item: Rim Plate Recalled by I.T.S. GmbH Due to The titanium implant has the wrong...

The Issue: The titanium implant has the wrong article number laser marked on it.

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

Class II — Potential Health HazardOngoing
DrugMay 9, 2019· American Health Packaging

Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...

The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2019· American Health Packaging

Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...

The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 8, 2019· Xhale Assurance, Inc.

Recalled Item: Nasal Alar SpO2 Sensor Recalled by Xhale Assurance, Inc. Due to These...

The Issue: These Instructions for Use has missing instructions related to the checking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part Recalled by...

The Issue: User may suffer an electric shock when coming in contact with the exposed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· NeuroLogica Corporation

Recalled Item: Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The Recalled...

The Issue: Potential issue related to the operation of the safety latch within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· Becton Dickinson & Company

Recalled Item: Alaris Pump Infusion Set Recalled by Becton Dickinson & Company Due to An...

The Issue: An incomplete occlusion can be caused by a variation in the wall thickness...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 6, 2019· Qiagen Sciences, Inc.

Recalled Item: RNeasy DSP FFPE Kit (48) Recalled by Qiagen Sciences, Inc. Due to The...

The Issue: The deparaffinization solution contains a contaminant, which leads to...

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

Class II — Potential Health HazardOngoing
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10089 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10084 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10079 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10037 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10191 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10116 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10149 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund