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. 2,340 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,340 in last 12 months

Showing 3582135840 of 48,326 recalls

Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: MAHURKAR"* 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2015· Taro Pharmaceuticals, Inc.

Recalled Item: Topicort (desoximetasone) Topical Spray Recalled by Taro Pharmaceuticals,...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2015· Natus Medical Incorporated

Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...

The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...

The Issue: A software fix has been released to prevent automatic movement resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2015· Leica Microsystems, Inc.

Recalled Item: The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology...

The Issue: The Leica ASP200S/ASP300S Tissue Processor have an incorrect internal wiring...

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

Class III — Low RiskOngoing
Medical DeviceAugust 5, 2015· Biomet Spine, LLC

Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling

The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

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

Class II — Potential Health HazardOngoing
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 4, 2015· MicroPort Orthopedics, Inc.

Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...

The Issue: Unexpected rate of postoperative fractures resulting in the need for...

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

Class I — Serious Health HazardOngoing