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. 2,101 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,101 in last 12 months

Showing 1500115020 of 30,032 recalls

Medical DeviceMarch 12, 2019· Beaver Visitec

Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling

The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...

The Issue: One of the software algorithms used to detect sample dispense errors was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Brainlab AG

Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...

The Issue: There is a potential for an incorrect dose distribution calculation by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades:Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Blades Monopolar Recalled by Gyrus ACMI, Inc. Due to Olympus...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Malleable Recalled by Gyrus ACMI, Inc. Due to Olympus Diego...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Olympus Diego Elite Console MDCONS 100 Recalled by Gyrus ACMI, Inc. Due to...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· ulrich medical USA Inc

Recalled Item: ULRICH Torque Limiting Handle for use with a Set Screw Recalled by ulrich...

The Issue: Certain Torque Limiting Handles in the field are beyond their 3 year...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25 Recalled by Becton...

The Issue: BD PAS received customer complaints indicating the absence of the bevel on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Abbott Gmbh & Co. KG

Recalled Item: Abbott Alinity ci-series System Control Module software version 2.5.1...

The Issue: Potential performance issues in the Alinity-ci software version 2.5.1

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There were multiple issues identified in the system software which required...

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

Class II — Potential Health HazardOngoing