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 2288122900 of 48,326 recalls

Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 6cm - Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Insulet Corporation

Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...

The Issue: There is a potential for a communication interruption following a bolus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Anti-HAV IgM test System Recalled by Roche Diagnostics Corporation Due to...

The Issue: Potential for erroneous result messages for the Anti-HAV IgM assay when run...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Meridian Bioscience Inc

Recalled Item: PREMIER Cryptococcal Antigen Recalled by Meridian Bioscience Inc Due to An...

The Issue: An enzyme reagent included in the kit is not maintaining stability through...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Bilirubin Total Gen.3 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Tina-quant IgM Gen.2 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Lactate Gen.2 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
DrugDecember 17, 2018· Promise Pharmacy, LLC

Recalled Item: Ipamorelin Recalled by Promise Pharmacy, LLC Due to Lack of sterility assurance.

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2018· Promise Pharmacy, LLC

Recalled Item: Epithalon Recalled by Promise Pharmacy, LLC Due to Lack of sterility assurance.

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund