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. 2,043 recalls have been distributed to Illinois in the last 12 months.
Showing 20061–20080 of 30,032 recalls
Recalled Item: Walgreens At-Home A1C Test Kit Recalled by Polymer Technology Systems Due to...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...
The Issue: The interface between the TB3 back and tilt base can separate when tilted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...
The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specimen Gate Laboratory 5002-0180 Recalled by PerkinElmer Health Sciences,...
The Issue: Issue may cause eReports to consume an excessive amount of disk space...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A...
The Issue: A complaint of the PRO2 jaw breaking prior to surgery being performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Diagnostics Ammonia L3K¿ Assay Recalled by Sekisui Diagnostics...
The Issue: Certain lots are showing an atypical decrease in optical density (OD) over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 3620-100: Oasis dual chamber drain with in-line connectors...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 400 Series Express Drains as follows: 4000-100N Express...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentraLink¿ Data Management System Software Versions: v13x Recalled by...
The Issue: There is a remote possibility CentraLink may download an order to the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes VA Implant Rack for the Compact Distal Radius System Recalled by...
The Issue: The screw rack plate was assembled incorrectly which could cause the screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 16400 Express Mini 500 dry seal drain Product Recalled by...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.