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. 1,812 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,812 in last 12 months

Showing 2568125700 of 27,852 recalls

Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Short Product Code:...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci 5 mm Flared Instrument Cannulae for use with Recalled by Intuitive...

The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Recalled...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach...

The Issue: Product did not reach expected sterility assurance level

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Merge Healthcare, Inc.

Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Multiple studies were missing at a customer location that never made it to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· DePuy Orthopaedics, Inc.

Recalled Item: DePuy Glenosphere orientation guide Product Usage: The glenosphere...

The Issue: The Glenosphere Orientation Guide Instrument Used with the Delta XTEND...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· ConMed Corporation

Recalled Item: PadPro(R) Adult Radiotransparent Multifunction Electrodes Recalled by ConMed...

The Issue: ConMed was notified by the contract manufacturer that their wire/connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: Large Tear Cross Cut Rasp 14mm x 7mm Ref. 5100-37-114 Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - CLEAR-TRAC COMPLETE Recalled by Surgical Instrument Service And Savings,...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Cannulated Drill Bit for Mini TightRope Ref. AR-8911DC Lot Recalled by...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Average Medium Blade 9mm x 25mm x 0.38mm Ref. 2296-3-111 Lot 122590...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: GII QuickAnchor Plus Recalled by Surgical Instrument Service And Savings,...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: Harmonic ACE Ergonomically-Enhanced Curved Shear Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - ConMed Linvatec Spectrum II Suture Hook Crescent Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing