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. 2,713 recalls have been distributed to Illinois in the last 12 months.
Showing 34021–34040 of 55,304 recalls
Recalled Item: GlipiZIDE Extended-release tablets Recalled by Amerisource Health Services...
The Issue: Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 1.5 gram added to 5% Dextrose 500 mL Recalled by SCA...
The Issue: Presence of particulate matter - this recall is due to a recent Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 1.5 g added to 0.9% Sodium Chloride 250 Recalled by SCA...
The Issue: Presence of particulate matter - this recall is due to a recent Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 1.25 g added to 5% Dextrose 250 mL Bag For IV Use Only...
The Issue: Presence of particulate matter - this recall is due to a recent Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 750 mg added to 5% Dextrose 250 mL For IV Use Only Recalled...
The Issue: Presence of particulate matter - this recall is due to a recent Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 750 mg added to 250 mL 0.9% Sodium Chloride For IV Use Only...
The Issue: Presence of particulate matter - this recall is due to a recent Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CycloSPORINE Capsules Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradations Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis zee Recalled by Siemens Medical Solutions USA, Inc Due to Failures can...
The Issue: Failures can result due to a component defect on Artis zee systems with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD System Controller The HeartWare Ventricular Assist System...
The Issue: Product recall of all HVAD Controllers currently on the market and to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...
The Issue: The stopcock was found to have punctures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture Recalled by CP...
The Issue: The tensile strength minimum as directed by USP <881> was not met over the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XPT System Software Versions V1.0.1 Recalled by Siemens...
The Issue: Multiple software issues, which may affect the operation and workflow of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q Care Continue Care Kit for the non-ventilated patient Recalled by Sage...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.