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. 2,722 recalls have been distributed to Illinois in the last 12 months.
Showing 33161–33180 of 55,304 recalls
Recalled Item: Kemps Sweet Me Creamery Expresso Mocha Recalled by Kemps, LLC Due to Kemps...
The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kemps YO2 Frozen Yogurt Cold Brewed Coffee Recalled by Kemps, LLC Due to...
The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kemps Sweet Me Creamery Chocolate Peanut Butter Pretzel Recalled by Kemps,...
The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kemps YO2 Frozen Yogurt Very Vanilla Recalled by Kemps, LLC Due to Kemps is...
The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kemps Sweet Me Creamery Creamy Dark Chocolate Mint Recalled by Kemps, LLC...
The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kemps YO2 Frozen Yogurt Raspberry Cheesecake Recalled by Kemps, LLC Due to...
The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...
The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol (17-B-Estradiol Recalled by Spectrum Laboratory Products, Inc. Due...
The Issue: CGMP Deviations: these repackaged and redistributed products are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP...
The Issue: CGMP Deviations: these repackaged and redistributed products are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS Recalled by...
The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS...
The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beyond Beef Feisty Crumble Vegan Gluten-free Non-GMO Weight: 10 lbs....
The Issue: Undeclared peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sterile Aquasonic 100 Ultrasound Transmission Gel Recalled by Parker...
The Issue: There is a potential for the gel packets to have leaks in the packet seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.