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. 2,043 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,043 in last 12 months

Showing 1950119520 of 30,032 recalls

Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Ferno-Washington Inc

Recalled Item: Ferno PROFlexx¿ Model 28Z Chair Cot Recalled by Ferno-Washington Inc Due to...

The Issue: The recall was initiated as a result of the detection of an incorrect nut...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Ortho-Clinical Diagnostics

Recalled Item: enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software...

The Issue: Software anomaly; Thermo-Fisher Scientific initially discovered and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· BioMerieux SA

Recalled Item: NucliSENS Lysis Buffer Recalled by BioMerieux SA Due to Problem with colored...

The Issue: Problem with colored eluates for whole blood extractions

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: Specimen Gate Laboratory Recalled by PerkinElmer Life and Analytical...

The Issue: Potential for errors in patient results generated by the Specimen Gate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· Ulrich Medical USA Inc

Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...

The Issue: Surgical technique was revised to prevent static plate screws blocking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...

The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Integra LifeSciences Corp.

Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...

The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that in isolated cases when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing