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 2524125260 of 28,127 recalls

Medical DeviceAugust 26, 2013· Snug Seat Inc

Recalled Item: Crocodile (size 3) are two-armed Recalled by Snug Seat Inc Due to The bolts,...

The Issue: The bolts, which secure the handles, on the Crocodile (size 3) could break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Bayer Healthcare Llc

Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...

The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2013· Medtronic Xomed, Inc.

Recalled Item: Universal Titanium Prosthesis Recalled by Medtronic Xomed, Inc. Due to One...

The Issue: One lot of the product was assembled using the Cam Head version of the same...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· ITC-Nexus Dx

Recalled Item: Surgicutt fully automated incision making device for bleeding time...

The Issue: ITC has determined that the blade in their Surgicutt with Blotting Paper...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· Ebi, Llc

Recalled Item: BIOMET Spine Recalled by Ebi, Llc Due to Polaris Translation Screw Failures...

The Issue: Polaris Translation Screw Failures were recently reported to Biomet Spine....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Combo 2 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 1 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Breakpoint Combo 4 Sold outside of US Recalled by...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Urine Combo 4 Sold outside of US Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.33 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 2 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Breakpoint Combo 7 Product Usage:...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.12 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Combo 3 Sold outside of US only. Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 20, 2013· Bio-Rad Laboratories

Recalled Item: FSE Image Upgrade Kit Recalled by Bio-Rad Laboratories Due to The FSE Image...

The Issue: The FSE Image Upgrade kit (part 92019C) is recalled due to issue related to...

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

Class III — Low RiskOngoing
Medical DeviceAugust 20, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX Evolution System (Standard Q) The DRX-Evolution System...

The Issue: Carestream received a report of an exposure being initiated without a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHECK FastClix Lancing Device. It is intended for use in Recalled by...

The Issue: Internal Roche inspections have revealed that after the lancet is used for a...

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

Class II — Potential Health HazardOngoing