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. 2,409 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,409 in last 12 months

Showing 3682136840 of 49,990 recalls

FoodSeptember 1, 2015· Savannah-Imperial LP- Savannah Sugar Refinery

Recalled Item: West Creek Recalled by Savannah-Imperial LP- Savannah Sugar Due to Foreign...

The Issue: Foreign matter (blue fiber) detected in product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodSeptember 1, 2015· Savannah-Imperial LP- Savannah Sugar Refinery

Recalled Item: Imperial GMI Recalled by Savannah-Imperial LP- Savannah Sugar Due to Foreign...

The Issue: Foreign matter (blue fiber) detected in product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 1, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical LEEP REDIKIT-Used as a surgical preparatory kit for Loop...

The Issue: Kit Label incorrect :Labeled with Lidocaine HCI drug cartridges Lidocaine...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 1, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...

The Issue: An issue with a USB memory component contained within a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Medical Systems Duodenoscope Recalled by Fujifilm Medical Systems...

The Issue: A precautionary measure because the Duodenoscopes have been redesigned to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Knee Bicompartmental Knee Replacement System Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iTotal CR (Cruciate Retaining) Knee Replacement System-iTOTAL CR...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS Unicondylar Knee Replacement System iUNI G2 Recalled by ConforMIS,...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iDUO G2 Recalled by ConforMIS, Inc. Due to May contain small...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Beckman Coulter Inc.

Recalled Item: Access Free T3 Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter, Inc. is recalling Access Free T3 Reagent Kit because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing