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. 2,959 recalls have been distributed to Illinois in the last 12 months.
Showing 3361–3380 of 55,304 recalls
Recalled Item: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...
The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT ONES brand ROJO Recalled by The Karma Sauce Company LLC Due to Foreign...
The Issue: Possible foreign object contamination (plastic).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HOT ONES brand VERDE Recalled by The Karma Sauce Company LLC Due to Foreign...
The Issue: Possible foreign object contamination (plastic).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD ChloraPrep Clear 1mL Applicators Recalled by CareFusion 213, LLC Due to...
The Issue: Non-Sterility: contamination of Aspergillus penicillioides, due to breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Airway adapter does not meet specification and may break off when attaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Airway adapter does not meet specification and may break off when attaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kids by babyganics SPF 50 mineral sunscreen totally tropical (titanium...
The Issue: Chemical Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Mislabeling
The Issue: Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5% Recalled...
The Issue: Chemical Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proxima Drape labeled as PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ORTHO TRAUMA CDS Recalled by MEDLINE INDUSTRIES, LP...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.