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. 2,890 recalls have been distributed to Illinois in the last 12 months.
Showing 10841–10860 of 30,032 recalls
Recalled Item: INJECTOR FORCEMAX SIF 270CM 23G 4MM Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 6MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 5MMx 21G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-203 GUIDE SHEATH Kit 2.6MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 23G 6MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 23G 3MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...
The Issue: The Quality Control (QC) card has a label error for the standard deviation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tourni-Cot - Universal Recalled by Mar-Med Co Due to A failure can occur if...
The Issue: A failure can occur if the user attempts to remove the device by partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm...
The Issue: Potential for the battery to lose its ability to be recharged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metalogix Self-Drill Half-Pin Recalled by New Standard Device Inc Due to...
The Issue: Complaints were received for Self-drill Half-Pin tip breakages occurring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS Incisive Computed tomography X-ray system Incisive CT Software...
The Issue: Patient tabletop moved out to the home position during scan initialization,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...
The Issue: Control panel arm assembly could have missing or loose screws where undue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. Clavicle Plating System Recalled by Biomet, Inc. Due to The...
The Issue: The instruments may become cold welded together when the drill is inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN Recalled by Combat...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Hypodermic Syringe 10 ml Recalled by Becton Dickinson & Company Due to...
The Issue: The product packaging for the 10 ml eccentric tip syringe may exhibit open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valkyrie LTOWB Collection (P/N 80-820 Recalled by Combat Medical Systems,...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Recalled by...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution: The IACS is Recalled...
The Issue: The Infinity M540 patient monitor may randomly reboot due to an error to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Recalled...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.