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. 2,115 recalls have been distributed to Illinois in the last 12 months.
Showing 13921–13940 of 30,032 recalls
Recalled Item: Kit BD Max Vaginal Panel Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 2 EU LUO Recalled by Becton Dickinson & Co. Due to The...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max CT/GC/TV Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Cdiff EU Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max GC RT PCR Assay Recalled by Becton Dickinson & Co. Due to The...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Parasite Panel EU Recalled by Becton Dickinson & Co. Due...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 2 USA Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Bacterial Panel EU Recalled by Becton Dickinson & Co. Due...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max MRSA XT Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukushima suction tubes Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: There was incorrect raw material used in the production of the identified lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The...
The Issue: Non-conforming devices are identified, which may not have been included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 05031656160 Recalled by Roche...
The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 07251670190 Recalled by Roche...
The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion systems with software version R1.2 -Interventional...
The Issue: The cold restart of Azurion R1.2 systems may take up to 7 minutes if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817 Recalled by...
The Issue: Supplier initiated recall of the GRIPPER Needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Flush Kit/Blood Draw Product Code: DT19335 Recalled by Centurion...
The Issue: Supplier initiated recall of the GRIPPER Needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Recalled by Centurion Medical Products Corporation Due to Supplier...
The Issue: Supplier initiated recall of the GRIPPER Needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port full Access Tray Product Code: DT19330 Recalled by Centurion Medical...
The Issue: Supplier initiated recall of the GRIPPER Needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage:...
The Issue: Negative Bias with Lot EA9227.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.