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. 2,932 recalls have been distributed to Illinois in the last 12 months.
Showing 6001–6020 of 55,304 recalls
Recalled Item: Labetalol Hydrochloride Injection Recalled by Pfizer Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Pfizer Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pink Luminous Breast Recalled by Silkprousa LLC Due to Firm is marketing and...
The Issue: Firm is marketing and distributing the Pink Luminous Breast device without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Queso Chonero Special White Cheese Recalled by EL CANGREJO GUAYACO LLC Due...
The Issue: The product is positive for Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Universal Bakery Organic Aussie Bites Recalled by Best Express Foods, Inc....
The Issue: Product is labeled as gluten free but consumer advocacy group testing...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tivicay PD (dolutegravir) 5mg Tablets for Oral Suspension Recalled by...
The Issue: Labeling: Incorrect Lot and/or Expiration Date: The carton has incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to...
The Issue: Electroneurodiagnostic medical device may contain a defective printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...
The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...
The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System Recalled by...
The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Recalled by...
The Issue: Siemens Healthineers has identified an issue with the RAPIDPoint500e system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RingLoc Bi-Polar Hip System Acetabular Cup Recalled by Biomet, Inc. Due to...
The Issue: 41 mm acetabular outer heads were potentially assembled with a 42 mm locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for...
The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol Transdermal System Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Transdermal System Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.