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. 2,694 recalls have been distributed to Illinois in the last 12 months.
Showing 37721–37740 of 55,304 recalls
Recalled Item: Candy Frozen Cookie Pucks 0.75oz Recalled by CSM Bakery Products NA Due to...
The Issue: Undeclared allergen; Peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FLIK Recalled by CSM Bakery Products NA Due to Undeclared Allergen
The Issue: Undeclared allergen; Peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Macadamia Nut Cookie with White Drops Recalled by CSM Bakery Products NA Due...
The Issue: Undeclared allergen; Peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...
The Issue: The latches of the frame adapter can be locked even if the locating pins of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional Recalled...
The Issue: The Surgical Table Cushion (HybriGel Pads) could potentially contain staples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...
The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...
The Issue: Defective Container: Excess lidding material accumulation between the seal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TM CR TIB SZ 3 C-H Recalled by Zimmer Trabecular Metal Technology, Inc. Due...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TM LPS TIB SZ 3 C/D Recalled by Zimmer Trabecular Metal Technology, Inc. Due...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision RFD Recalled by Ziehm Imaging Inc Due to Malfunction of the...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TM MONO TIB STR GRN SZ 5 - 00588606510 TM Recalled by Zimmer Trabecular...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slip-Cath Beacon Tip Catheter Catheter Recalled by Cook Inc. Due to Increase...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.