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 2300123020 of 48,326 recalls

Medical DeviceDecember 5, 2018· Medela Inc

Recalled Item: Breast Milk Transfer Lid for use with Oral Syringe Connectors Model:...

The Issue: The sterility may be compromised due to a potential breach in the packaging,...

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

Class III — Low RiskOngoing
Medical DeviceDecember 5, 2018· Exactech, Inc.

Recalled Item: Equinoxe Preserve Humeral Stem Recalled by Exactech, Inc. Due to Possibility...

The Issue: Possibility that the Equinoxe Preserve Humeral Stem, 8mm, was inadvertently...

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

Class II — Potential Health HazardOngoing
DrugDecember 4, 2018· Epic Pharma, LLC

Recalled Item: Estradiol Tablets Recalled by Epic Pharma, LLC Due to Presence of foreign...

The Issue: Presence of foreign tablet/capsule: A single foreign tablet was found in...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 4, 2018· Earthworks Health

Recalled Item: Diatomaceous Earth packaged in the following ways: 1) Perma-Guard Recalled...

The Issue: Product contains elevated levels of lead, arsenic, and chromium: potentially...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 4, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...

The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...

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

Class III — Low RiskOngoing
Medical DeviceDecember 4, 2018· Agfa-Gevaert, N.V.

Recalled Item: DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by...

The Issue: After an upgrade of the software of the Overhead Tube Crane, there were...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2018· Conformis, Inc.

Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...

The Issue: The kits were prepared with incorrect patient ID labels and may contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2018· PENTAX of America Inc

Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...

The Issue: The Controller does not detect overpressure in the balloon during the...

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

Class II — Potential Health HazardOngoing
DrugNovember 30, 2018· VistaPharm, Inc.

Recalled Item: NYSTATIN Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

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

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

Class III — Low RiskOngoing
Refund
DrugNovember 30, 2018· Aurobindo Pharma USA Inc.

Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Aurobindo Pharma USA...

The Issue: Discoloration: This product is being recalled due to a confirmed pharmacist...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 30, 2018· Philips Medical Systems Nederlands

Recalled Item: Azurion lnterventional Fluoroscopic X-ray System Recalled by Philips Medical...

The Issue: Philips has discovered through customer complaints and internal testing an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Beaver Visitec

Recalled Item: BVI Visitec Soft Tip Cannula Recalled by Beaver Visitec Due to Certain lots...

The Issue: Certain lots are missing a protective sheath component over the silicone...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Siemens Biograph Horizon PET/CT System Recalled by Siemens Medical Solutions...

The Issue: Improper design or specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Tosoh Bioscience Inc

Recalled Item: ST AIA-PACK ACTH (ACTH: Adrenocorticotropic Hormone) is designed for IN...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE Recalled by...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Tosoh Bioscience Inc

Recalled Item: ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC Recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Tosoh Bioscience Inc

Recalled Item: ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC Recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Tosoh Bioscience Inc

Recalled Item: ST AIA-PACK FT3 (FT3: Free Triiodothyronine) is designed for IN Recalled by...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC Recalled by...

The Issue: Potential for fluorescein interference to cause inaccurately elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: Vitros Myoglobin Calibrators Recalled by Ortho Clinical Diagnostics Inc Due...

The Issue: A stability issue in the calibrators may cause calibration failures or...

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

Class II — Potential Health HazardOngoing