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 2694126960 of 28,127 recalls

Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Greatbatch Medical

Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...

The Issue: We are notifying you of a potential interaction between therapeutic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Oncology...

The Issue: An anomaly has been identified with the ARIA Oncology Information System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray V12 Size: 320 mm X 320 mm X 450 Recalled by Mindray DS USA, Inc....

The Issue: Mindray has identified an issue with the V Series Monitor where the monitors...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Centrifugal System Control module System 9000 The Sarns Centrifugal...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2012· Zimmer, Inc.

Recalled Item: NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The...

The Issue: Zimmer is initiating a lot specific recall of the NexGen¿ Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Advanced Sterilization Products

Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima 200amx Mobile general purpose radiographic imaging of...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Captiva Spine, Inc

Recalled Item: CapLOX II Final Torque Driver Recalled by Captiva Spine, Inc Due to Captiva...

The Issue: Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 200amx with digital upgrade Mobile general Recalled...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Sorin Group USA, Inc.

Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Sorin Group USA, Inc.

Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Medline Industries Inc

Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...

The Issue: The Back Table Cover component in the custom pack was placed in the...

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

Class II — Potential Health HazardOngoing