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 2542125440 of 28,127 recalls

Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: Pipeline Embolization Device (PED) The Pipeline Embolization Device is...

The Issue: Covidien Neurovascular has initiated the recall of several lots of Pipeline...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR V-Patch Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR TacShield Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Blue Belt Technologies MN

Recalled Item: Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue...

The Issue: Blue Belt Technologies is recalling sterile Monitor Drapes used with their...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 300 and ACL TOP 300 CTS (Japan) Recalled by Instrumentation...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2013· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Disposable Temperature Probes Recalled by Vital Signs Devices, a GE...

The Issue: GE Healthcare has become aware of a potential safety issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...

The Issue: Siemens has become aware of a customer complaint concerning the rail...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2013· Aspen Surgical Products, Inc.

Recalled Item: Distributed in USA: Product Number: 40-2894: Reinforced Wound Closure...

The Issue: Aspen Surgical is recalling Wound Closures because firm could not confirm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Custom Perfusion System with Trillium BioSurface (a polymer...

The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2013· Arrow International Inc

Recalled Item: Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter...

The Issue: Arrow is recalling the Arrowgard Blue Plus Antimicrobial Multi-lumen Central...

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

Class II — Potential Health HazardOngoing