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. 2,475 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,475 in last 12 months

Showing 2186121880 of 28,127 recalls

Medical DeviceMay 11, 2015· Orthofix, Inc

Recalled Item: ORTHOFIX Centurion POCT System Drill Guide PN 69-1010 and PN Recalled by...

The Issue: There is a possibility that the thumb button remains in the depressed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2015· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 220-230V Recalled by...

The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2015· Abbott Laboratories

Recalled Item: Alkaline Wash Recalled by Abbott Laboratories Due to The product is leaking...

The Issue: The product is leaking from the cap and crystallization was noted as present...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2015· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 208V Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 0210-312-000-Woundcare Replacement kit with soft tip Recalled by Stryker...

The Issue: Potential sterility breach in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...

The Issue: Reports where patients who recently switched from the current Shiley...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: RaySearch RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: RaySearch Laboratories AB became aware of an issue with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...

The Issue: Reports where patients who recently switched from the current Shiley...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2015· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...

The Issue: Potential lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Ethicon, Inc.

Recalled Item: Ethicon Fast Absorbing Plain Gut - MultiPass Needles Recalled by Ethicon,...

The Issue: Ethicon Fast Absorbing Surgical Gut (Plain) Suture is being recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...

The Issue: Potential lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Triglycerides GPO. In vitro test for the quantitative determination of...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: HDL-Cholesterol gen.3. For the quantitative determination of high-density...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Lactate. Intended for use on COBAS INTEGRA 800 and 400 plus systems Recalled...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing