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. 2,644 recalls have been distributed to Iowa in the last 12 months.
Showing 3721–3740 of 49,990 recalls
Recalled Item: OEC 9800 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685....
The Issue: A software bug within the Gen 2 StatStrip Hospital Meter firmware leads to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog...
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683....
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216 Recalled by...
The Issue: The following four issues are included: 1. Certain Channel Settings may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine DR Capsules USP 60 mg Recalled by Rising Pharma Holding, Inc. Due...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Rising Pharma Holding,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Rising Pharma Holding,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VACUETTE SAFELINK Recalled by Greiner Bio-One GmbH Due to The VACUETTE...
The Issue: The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo USA, Inc. Due to...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo USA, Inc. Due to...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablet Recalled by Endo USA, Inc. Due to...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.