Product Recalls in Oregon

Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,457 in last 12 months

Showing 2794127960 of 28,488 recalls

Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT-DR VANTRIGHT 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: CPB CATHETER KIT-DR GERHARDT 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
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CUSTOM CPB CATHETER KIT-DR. 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: XC HEART/LUNG PACK W/SX25RX 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: X-COATED SMALL PATIENT PACK 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 HIGH-FLOW AORTIC ARCH CANNULA: 5.2 MM (16 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
Medical DeviceMay 9, 2012· Natus Medical Incorporated

Recalled Item: The product has the Catalogue/Part number 60010. Olympic Cool-Cap System...

The Issue: The Olympic Cool-Cap's Control Module has experienced a frozen screen during...

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

Class I — Serious 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: CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Recalled by...

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: 8.0 MM (24 FR) WITH 3/8" CONNECTOR Recalled...

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· Terumo Cardiovascular Systems Corporation

Recalled Item: 24FR FLEX ART CANN NON STERILE. The Sarns High Flow Recalled by Terumo...

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· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 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
Medical DeviceMay 9, 2012· RAYSEARCH LABORATORIES AB

Recalled Item: Brand name: RayStation. Generic name: Treatment Planning System. Software...

The Issue: The firm decided to recall when an issue was found with the dose calculation...

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 FX25RW H/L PACK 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: X-COATED SMALL PATIENT PACK 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· Covidien LP

Recalled Item: Covidien ROTICULATOR 30-4.8 Single Use Stapler REF# 017617 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: SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 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
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...

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 TRANSPLANT PACK 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