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. 1,028 recalls have been distributed to Illinois in the last 12 months.
Showing 39761–39780 of 55,304 recalls
Recalled Item: MiniArc Pro Single incision Sling System Recalled by Astora Due to The lot...
The Issue: The lot number on the outer carton label did not match the lot number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cavity 8 Gauge Spine Wand indicated for resection Recalled by ArthroCare...
The Issue: There is cracking in the tray when the device is snapped into place. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mountain Mix 2oz bag Recalled by Kanan Enterprises, Inc. Due to Undeclared Milk
The Issue: The firm was notified that the product contains undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: David Trail Mix Sweet & Salty individual plastic bags net Recalled by...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kings fresh & Delicious Cashews & Sweeties Net Wt. 14oz. Recalled by Kanan...
The Issue: The firm was notified that the product contains undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sweet & Salty Mix 2.75oz Tube Bag Recalled by Kanan Enterprises, Inc. Due to...
The Issue: The firm was notified that the product contains undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152...
The Issue: Medtronic has discovered that select lots of the Amphirion Deep PTA Balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units) Recalled...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon GranuFlo Dissolution Unit - P/N G047-80101. For...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential issue with routine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon Dry Acid Dissolution Unit Recalled by Fresenius Medical...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iOS Galileo Application Version 1.1.1 or lower that programs the Recalled by...
The Issue: A software issue can make the foot move into dorsiflexion, unnoticed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The...
The Issue: Incorrect use of T-Piece resuscitators will result in complete occlusion of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans Recalled...
The Issue: Monitor may shut down unintentionally without restarting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 6F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Needle Guide Starter Kit Recalled by Civco Medical Instruments Co....
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Medical CXI Support Catheter 2.6FR curved catheter and 4.0FR Recalled...
The Issue: Cook Medical has received six product complaints associated with reports of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 7F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 5F Recalled by LeMaitre Vascular,...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.