Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,447 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,447 in last 12 months

Showing 2758127600 of 28,127 recalls

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: 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· Covidien LP

Recalled Item: Covidien ROTICULATOR 30-3.5 Single Use Stapler REF# 017615 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: 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· 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: CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch 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 55-4.8 Single Use Stapler REF# 017614 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: MAYO MN XCOATED 3/8X1/2 AV 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: CPB CATHETER KIT- DR.VAN TRIGHT. The Sarns High Flow Aortic 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· 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: 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: 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: 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· Covidien LP

Recalled Item: Covidien ROTICULATOR 55-3.5 Single Use Stapler REF# 017612 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 FLEXIBLE ARTERIAL CANNULA: 6.7 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 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· 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: 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