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. 1,839 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,839 in last 12 months

Showing 4236142380 of 55,304 recalls

Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Shoulder Arthroscopy Pack Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: D&C/Cysto Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Abdominoplasty Tray Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Student Pack-NS Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Head and Neck Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Transvaginal Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Spine Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Foot Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Eye Plastic Tray Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2015· Spacelabs Healthcare Inc

Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...

The Issue: Modules resetting. This failure mode happens when the Spacelabs Command...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2015· Zimmer Surgical Inc

Recalled Item: Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer...

The Issue: Devices were placed in a shipper carton without the appropriate number of...

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

Class III — Low RiskOngoing
DrugApril 21, 2015· Alvogen, Inc

Recalled Item: NITROFURANTOIN MONOHYDRATE/MACROCRYSTALS CAPSULES Recalled by Alvogen, Inc...

The Issue: Failed Dissolution Specification; 6 month time point

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2015· Akorn, Inc.

Recalled Item: IC-GREEN (indocyanine green for injection Recalled by Akorn, Inc. Due to...

The Issue: Subpotent Drug: Low out-of-specification potency result of the drug product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: ACL Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Suction Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Glaucoma Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Knee Arthro Pack and Knee Arthro Pack II - contains Recalled by Stradis...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Lima Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Mississippi Pack - contains Devon Light Glove Used during surgery Recalled...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Arthroscopy Pack - contains Devon Light Glove Used during surgery Recalled...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing