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. 2,932 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,932 in last 12 months

Showing 54415460 of 55,304 recalls

Medical DeviceJuly 17, 2024· Boston Scientific Neuromodulation Corporation

Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...

The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter Healthcare...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Mazor Robotics Ltd

Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...

The Issue: Software anomalies which can result in two separate issues: A lagging screen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Firm has released a...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25GA VALVED ENTRY SYSTEM Recalled by Alcon Research LLC Due to...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: TOTAL PLUS Recalled by Alcon Research LLC Due to Alcon has...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ TOTALPLUSr CP PAK 20K CPM BWV .9 Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: A-OK SATINSLIT FULL HANDLE2.75MM ANG SG Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE3.0MM ANG DUAL Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: TOTALPLUS Recalled by Alcon Research LLC Due to Alcon has...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Software...

The Issue: Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT HP2 DB SLIT 3.2MM ANGCE Recalled by...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: 20 Gauge V-Lance Knife Model/Catalog Number:...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: ClearCut S Safety Sideport Knife 1.2mm Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY SLIT SB Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+TTLPL VPK 20000CPM BEV VAL Model/Catalog Number: 8065753106...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: A-OK SATINCRESCENT FULL HANDLE2.3MM ANG...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing