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. 1,723 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,723 in last 12 months

Showing 4546145480 of 49,990 recalls

Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Philips Healthcare Inc.

Recalled Item: Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography...

The Issue: The Instructions for Use (IFU) for the MobileDiagnost wDR fails to comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· GE Healthcare It

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: GE has recently become aware of potential issues due to out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Bethel 30 capsules Recalled by Bethel Nutritional Consulting, Inc Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 25 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Biomet 3i, LLC

Recalled Item: Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm Recalled by Biomet...

The Issue: One of the dental implants do not have the internal hex feature. One of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Radiometer America Inc

Recalled Item: pO2 D999 membrane units. Distributed by Radiometer America Recalled by...

The Issue: RADIOMETER became aware that the regarded lot pO2 units 942-042R0971 were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Biomet 3i, LLC

Recalled Item: Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product...

The Issue: One of the dental implants do not have the internal hex feature. One of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 5 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Cardinal BI Stat Biological Test Pack with Instant Readout Integrator...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Staar Surgical Co.

Recalled Item: Afinity CQ2015A Intraocular Lens The visual correction of aphakia in...

The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Steam Biological Indicators Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing