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. 2,909 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,909 in last 12 months

Showing 1052110540 of 30,032 recalls

Medical DeviceFebruary 26, 2021· Heartware, Inc.

Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...

The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 26, 2021· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...

The Issue: Their is a potential that Video Processor/Illuminators may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Hologic, Inc

Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to There is a...

The Issue: There is a potential for tube trays to leak which could potentially result...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Covidien Llc

Recalled Item: CF Delivery Dev Caps Bravo x5 Recalled by Covidien Llc Due to The capsule...

The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Covidien Llc

Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...

The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Interventional Fluoroscopic X-Ray System - Product Usage: developed for...

The Issue: Siemens has become aware of a potential issue in which the imaging system...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· CAIRE DIAGNOSTICS INC

Recalled Item: CAIRE DIAGNOSTICS FenomPro SN ***** - Product Usage: a portable Recalled by...

The Issue: Erroneously high FeNO levels which may contribute to premature...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Accuray Incorporated

Recalled Item: CyberKnife Treatment Delivery System - Product Usage: indicated for...

The Issue: The set screws that connect the Standard Treatment Couch linkage arm to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· BioMedical Equipment Service Co (BMES)

Recalled Item: Alaris Infusion Pump Module Recalled by BioMedical Equipment Service Co...

The Issue: Bezel repair parts used, not by the original manufacturer, to service and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2021· Dutch Ophthalmic USA, Inc.

Recalled Item: Disposable Replacement Backflush Brush Needles (23 gauge/0.6mm)-for use in...

The Issue: Mislabeled: 1281.B1D Disposable Replacement Backflush Brush Needles label...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit - Product Usage: intended for use in Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus MNC Apheresis Kit - Double Needle - Product Usage: Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit Therapeutics - Product Usage: intended for use Recalled...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Biocare Medical, LLC

Recalled Item: BIOCARE Medical Recalled by Biocare Medical, LLC Due to Their is a potential...

The Issue: Their is a potential that the automated staining instrument with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Bulk Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Sterile Recalled by Cardinal Health 200, LLC Due...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Bulk Non-Sterile Recalled by Cardinal Health 200, LLC...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Access Vascular, Inc.

Recalled Item: Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142...

The Issue: Scalpel and StatLock components packaged with specific lots of the HydroPICC...

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

Class II — Potential Health HazardOngoing