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. 2,357 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,357 in last 12 months

Showing 4886148880 of 49,990 recalls

Medical DeviceJune 15, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...

The Issue: Hitachi discovered a software error with a feature called Multi-Planar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Angiodynamics Worldwide Headquarters

Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...

The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Octane-C Cervical Recalled by Exactech, Inc. Due to Exactech, Inc. initiated...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
DrugJune 14, 2012· Dukal Corp.

Recalled Item: ZEE Antiseptic Wipes Recalled by Dukal Corp. Due to Microbial contamination...

The Issue: Microbial contamination of Non Sterile Product; contamination with...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2012· Dukal Corp.

Recalled Item: Dukal Corporation BZK Swab Recalled by Dukal Corp. Due to Microbial...

The Issue: Microbial contamination of Non Sterile Product; contamination with...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2012· Kimberly-Clark Corporation

Recalled Item: Kleenex Luxury Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation...

The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2012· Kimberly-Clark Corporation

Recalled Item: Kleenex Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation Due to...

The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2012· KOREAN FARM, INC.

Recalled Item: IQF Oysters 3lbs Recalled by KOREAN FARM, INC. Due to Korean Farm is...

The Issue: Korean Farm is recalling Assi Brand Korean Oysters because they have been...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 14, 2012· Integra Life Sci.

Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...

The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2012· Philips Healthcare Inc.

Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...

The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...

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

Class II — Potential Health HazardOngoing
FoodJune 13, 2012· Pacific Giant, Inc

Recalled Item: Ocean Manna Korean IQF Oysters Recalled by Pacific Giant, Inc Due to Pacific...

The Issue: Pacific Giant is recalling all frozen (IQF) oyster meat and 1/2 shell...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing