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. 1,965 recalls have been distributed to Illinois in the last 12 months.
Showing 28141–28160 of 55,304 recalls
Recalled Item: Milk Chocolate Covered Fudge Bites Recalled by Morley Candy Makers, Inc. Due...
The Issue: Morley Candy Makers, Inc. initiated a voluntary recall of Sanders Milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...
The Issue: Resuspension problems: Out of specification for appearance and resuspendability.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X-Jow (menthol USP) Pain Gel Recalled by Shadow Holdings DBA Bocchi Labs Due...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave 3 Step Shaving System Recalled by Shadow Holdings DBA Bocchi Labs...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave (salicylic acid) Shave Cream Acne Shield Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis zee systems with Laird Cooling Unit for SSFD: Material Recalled by...
The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis with Laird Cooling Unit for SSFD: Material # Recalled by Siemens...
The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...
The Issue: Product may contain unlabeled coconut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Allergan Taytulla Softgel Capsules Recalled by Allergan, PLC. Due to...
The Issue: Contraceptive Tablets Out of Sequence.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK 5 Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT-Check MANUAL RESUSCITATOR / VENTILATOR Recalled by Sun Med, LLC Due to...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS Tiro Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.