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 20621–20640 of 55,304 recalls
Recalled Item: GEM Microvascular Anastomotic Coupler Devices s intended to be used Recalled...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips V60 Ventilators with Power Management PCBA part number 1055906...
The Issue: Solder connection failure on Power Management printed circuit board assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: natus newborn care Olympic Brainz Monitor Recalled by Natus Neurology DBA...
The Issue: The OBM system functional test (impedance and noise) was not carried out on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket Recalled...
The Issue: Potential for the weld to fail at the pivot point of the monitor bracket....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrediniSONE Tablets Recalled by Par Pharmaceutical Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STA - Deficient VIII Recalled by Diagnostica Stago, Inc. Due to A risk of...
The Issue: A risk of sample-to-sample cross-contamination of Emicizumab for factor VIII...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation standalone software treatment planning system Recalled by...
The Issue: Due to physical limitations of the treatment machine, the maximum field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEPPERMINT LIP MOISTURIZER (oxybenzone (4%) and Octinoxate (7%) SPF 15...
The Issue: Superpotent drug: This lot of SPF containing lip balm contains up to 150% of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vita Wild Herring in Wine Sauce 32oz plastic jar Recalled by Vita Food...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System Recalled by Capintec Inc Due to It is...
The Issue: It is possible that the collimators have screw hole locations that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa and Levodopa Tablets Recalled by Mayne Pharma Inc Due to Product...
The Issue: Product Mix-Up: A foreign tablet was found in bottle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature's Earthly Choice Organic Lentil Trio product containing a blend...
The Issue: Gluten-Free lentils product tested positive for gluten and some pouches were...
Recommended Action: Do not consume. Return to store for a refund or discard.