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. 2,776 recalls have been distributed to Illinois in the last 12 months.
Showing 20861–20880 of 55,304 recalls
Recalled Item: Southern Sisters Gourmet Shrimp and Stone-Ground Grits Recalled by Southern...
The Issue: Undeclared allergen: Milk. Undeclared colors: Yellow #5 and #6.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Taco Soup Recalled by Southern Sisters Gourmet Due...
The Issue: Undeclared allergens: Milk and Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Crab Cake Mix Recalled by Southern Sisters Gourmet...
The Issue: Undeclared allergens: Wheat and Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Oven Fried Chicken Recalled by Southern Sisters...
The Issue: Undeclared allergen: Wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Caramel Apple Cobbler Recalled by Southern Sisters...
The Issue: Undeclared allergen: Wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Beepa's Original Goulash Starter Recalled by Beepas LLC Due to Undeclared Milk
The Issue: Beepa's Goulash Starter contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedicle Screws Recalled by Medicrea International Due to An internal...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer Recalled...
The Issue: When using the Rotor-Gene Q with Software version 2.3.4 completing a LIMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iliac Screws Recalled by Medicrea International Due to An internal component...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video...
The Issue: Blades do not fit the McGRATH MAC video laryngoscope handle or were tight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protective Cover Vivo 55/65 (Used for Vivo 50/65) Recalled by Breas Medical,...
The Issue: The outlet hole of the exhalation valve control pressure tube on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...
The Issue: CGMP deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...
The Issue: CGMP deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...
The Issue: GMP Deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...
The Issue: GMP Deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Truliant Splined Stem Extension Recalled by Exactech, Inc. Due to These...
The Issue: These Truliant Splined Stem Extension, 18mm x 120mm were found to have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans...
The Issue: FridaBaby has been made aware through customer reports that the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solifenacin Succinate Tablets Recalled by Breckenridge Pharmaceutical, Inc...
The Issue: CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.