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. 2,915 recalls have been distributed to Illinois in the last 12 months.
Showing 8781–8800 of 30,032 recalls
Recalled Item: SIGNA Excite 3T. Magnetic Resonance Imaging System Recalled by GE...
The Issue: There is potential for the images to be flipped left to right.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T and 3.0T SIGNA HDx Recalled by GE Healthcare, LLC Due to There is...
The Issue: There is potential for the images to be flipped left to right.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signa 1.5T TwinSpeed Magnetic Resonance Imaging System Recalled by GE...
The Issue: There is potential for the images to be flipped left to right.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device products purchased from Family Dollar retail stores located...
The Issue: Potential exposure to rodents and rodent activity in the distribution center.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORAcollect RNA: ORE-100 Recalled by DNA Genotek Inc. Due to Evaporation of...
The Issue: Evaporation of stabilizing liquid reducing shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems...
The Issue: Potential for false positive results for SARS-CoV-2 in identified lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORAcollect Dx Recalled by DNA Genotek Inc. Due to Evaporation of stabilizing...
The Issue: Evaporation of stabilizing liquid reducing shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIPOSORBER System Recalled by Kaneka America Corp Due to Labeling change to...
The Issue: Labeling change to due to the risk of severe anaphylactoid reactions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Mount Clamp Assembly (table adapter component) Recalled by Deerfield...
The Issue: Reports have been received that after normal or routine lateral forces are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter IRISpec CA/CB/CC control Recalled by Beckman Coulter, Inc....
The Issue: IRISpec CA failures for glucose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to The photomultiplier...
The Issue: The photomultiplier tube, may have compromised functionality in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProteusPLUS and ProteusONE- designed to produce and deliver a proton...
The Issue: When resuming from a beam pause, the Proton Therapy System does not verify...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET TRAUMA Drill Bit Recalled by Biomet, Inc. Due to Packaging of various...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Therapy Air Supply Unit Recalled by Baxter Healthcare Corporation...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Bariatric Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytocell 8 Square Template Slides (Glass)- microscope slides : PCN008...
The Issue: Labelled with an incorrect expiry date on the outer label with an extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN:...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Software 2.51.01 and Lower- intended for...
The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Trauma Recalled by Biomet, Inc. Due to Packaging of various implants...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.