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 3880138820 of 49,990 recalls

DrugApril 17, 2015· Valeant Pharmaceuticals North America LLC

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: High out of specification dissolution...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 17, 2015· Natar Foods, Inc.

Recalled Item: Dry Bream-lesh (Fish) Recalled by Natar Foods, Inc. Due to The product was...

The Issue: The product was found to be uneviscerated based on sampling and analysis by...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Surgical Set Up kit Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Biomet Cobalt-Chrome Femoral Components Recalled by Biomet, Inc. Due to...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Surgical Kit Sterile-Kits containing the Devon Light Glove Catalog...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Delivery/C-Section Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: ASC (Breast) Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Augmentation Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Mini-Kits Recalled by Covidien LLC Due to Devon Light Gloves contain splits...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Covidien Devon Light Gloves Recalled by Covidien LLC Due to Devon Light...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Hysto Pack Recalled by Covidien LLC Due to Devon Light Gloves contain splits...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Non Sterile Subassembly: Catalog Number/Description: SA1008 NONSTERILE...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Single Basin Kits Recalled by Covidien LLC Due to Devon Light Gloves contain...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· BioHorizons Implant Systems Inc

Recalled Item: Tapered HD Upgrade Set Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: BioHorizons Tapered HD Upgrade set was packaged with an incorrect drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: NS-3600-B LITE GLOVE 1000/CASE -Bulk Recalled by Covidien LLC Due to Devon...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Double Basin Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...

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

Class II — Potential Health HazardOngoing