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 2740127420 of 28,127 recalls

Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 220/240V. The Recalled by...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand Varian Eclipse Treatment Planning System for radiotherapy...

The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning (for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Cardiovascular Systems, Inc.

Recalled Item: CSI Stealth 360-degree Orbital Atherectomy Device (OAD) Recalled by...

The Issue: CSI has initiated a recall on specific lot numbers of Stealth 360-degree...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2012· DeRoyal Industries Inc

Recalled Item: Custom surgical kits and trays: GEO-MED TOTAL KNEE PACK PGYBK Recalled by...

The Issue: Surgical kits and trays contain Stryker Hytrel Togas which were recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Diagnostica Stago, Inc.

Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...

The Issue: Following a single customer complaint that incorrect INR values were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Octane-C Cervical Recalled by Exactech, Inc. Due to Exactech, Inc. initiated...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Angiodynamics Worldwide Headquarters

Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...

The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent...

The Issue: The recall was initiated because Carefusion has identified a potential risk...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...

The Issue: Hitachi discovered a software error with a feature called Multi-Planar...

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

Class II — Potential Health HazardOngoing