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. 1,973 recalls have been distributed to Illinois in the last 12 months.
Showing 26061–26080 of 30,032 recalls
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm)...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS Recalled by...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm Weck¿ Vista" Cannula-only Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port Short Length (53mm)...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm)...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12mm Weck¿ Vista" Cannula-only Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Universal Cannula Recalled by Teleflex Medical Due to...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIO Recalled by Teleflex Medical Due to The product did not meet minimum...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software...
The Issue: The System may go into a controlled failed state if a series of parameters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra CUSA Excel Disposable Wrench. Catalog Number C5601. The CUSA...
The Issue: Some 23 kHz Torque Wrenches were incorrectly assembled and contained a 36...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neusoft NeuViz 64 Multi-slice CT Scanner System Recalled by Neusoft Medical...
The Issue: The A-plane compensator is made of Teflon which will become fragile due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halogen Lamp component in RetCam 3 System - Clarity Medical Systems Recalled...
The Issue: One lot of Halogen lamps have the potential to fail sooner than the expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: A customer reported that after upgrading to software version 3.5.5 from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FB Reagent (). FB reagent is an additional test Recalled by BioMerieux SA...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NIH (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent (). The ZYM B reagent is Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....
The Issue: The outer package label contained the incorrect length of the device. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...
The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.