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. 2,964 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,964 in last 12 months

Showing 221240 of 30,032 recalls

Medical DeviceDecember 24, 2025· Medline Industries, LP

Recalled Item: Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG...

The Issue: Medline Industries, LP is issuing a recall for specific items and lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2025· Medline Industries, LP

Recalled Item: Medline medical convenience kits packaged as: STERILE RESUTURE PACK Recalled...

The Issue: Medline Industries, LP is issuing a recall for specific items and lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2025· Medline Industries, LP

Recalled Item: Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience...

The Issue: A smaller open suction catheter, the 8 Fr Suction Catheter, may have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2025· Medline Industries, LP

Recalled Item: Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY Recalled...

The Issue: Medline Industries, LP is issuing a recall for specific items and lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2025· Medline Industries, LP

Recalled Item: Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE...

The Issue: Medline Industries, LP is issuing a recall for specific items and lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2025· GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING

Recalled Item: GE Healthcare Omni Legend Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL...

The Issue: There is a potential intermittent issue on certain Omni Legend systems that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2025· Focalyx Technologies, LLC.

Recalled Item: Focalyx Fusion Recalled by Focalyx Technologies, LLC. Due to Software device...

The Issue: Software device that is an accessory for image-guided interventional and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2025· Beckman Coulter, Inc.

Recalled Item: CellMek SPS Sample Preparation System Recalled by Beckman Coulter, Inc. Due...

The Issue: Sample preparation system designed to automate staining, lysing, cell...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2025· Philips North America

Recalled Item: Patient Information Center iX Recalled by Philips North America Due to A...

The Issue: A recent software (SW) patch modifies Mobile Event Notification filter...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters:...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters:...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· LSL Healthcare Inc.

Recalled Item: LSL Healthcare Recalled by LSL Healthcare Inc. Due to BD ChloraPrep Triple...

The Issue: BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Altruan GmbH

Recalled Item: Brand Name: Bisaf Strep A Self-Test. Test for detection of Recalled by...

The Issue: Product not cleared by the FDA.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing