Product Recalls in Illinois
Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,839 recalls have been distributed to Illinois in the last 12 months.
Showing 42461–42480 of 55,304 recalls
Recalled Item: Mallory/Head Primary Hip 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.
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.
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.
Recalled Item: MCK Maximum Congruent Knee 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.
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.
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.
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.
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.
Recalled Item: Hitachi Oasis MRI System Recalled by Hitachi Medical Systems America Inc Due...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon Oval MRI System Recalled by Hitachi Medical Systems America...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon MRI System Recalled by Hitachi Medical Systems America Inc...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Antacid Liquid Recalled by Tarmac...
The Issue: Products failed the Antimicrobial Effectiveness Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Comfort Gel Cherry Flavor Recalled by...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Cold Recalled by Reckitt Benckiser LLC Due to Labeling:...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Severe Congestion & Cough Recalled by Reckitt Benckiser LLC...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast-Max Cold & Sinus Recalled by Reckitt Benckiser LLC Due to...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Night Time Cold & Flu Recalled by Reckitt Benckiser LLC Due...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine HCl Chewable Tablet Recalled by Sandoz, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.