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. 1,799 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,799 in last 12 months

Showing 2730127320 of 27,852 recalls

Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 141F7. For...

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7P....

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HVF7P....

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131F7J....

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131F7P....

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151HF7....

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 volume imaging ultrasound systems at software versions VA16C...

The Issue: In some cases, the system is unable to capture a clip or image during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SPECIALTYCARE - HUDGENS. The Sarns High Flow Aortic Arch Cannula Recalled by...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Covidien LP

Recalled Item: Covidien ROTICULATOR 30-V3 Single Use Stapler REF# 017619 The RETICULA...

The Issue: Potential for the sterility barrier to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS ANTEGRADE: CARDIOPLEGIA CANNULA: ROOT INFUSION VENT/CATHETER WITH 14-...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT-DR BARTLES Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 7.3 MM (22 FR) 00 WITH 3/8" CONNECTOR...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing