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. 2,915 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,915 in last 12 months

Showing 83018320 of 30,032 recalls

Medical DeviceJune 1, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...

The Issue: An issue with propagation of treatment course information from RayStation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Ventana Medical Systems Inc

Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...

The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Spectranetics Corporation

Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to The...

The Issue: The LAS-100 Laser system may detect an inoperable hardware component during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Ultradent Products, Inc.

Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...

The Issue: SE primer may be missing some or all of the resin portion of the chemistry....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...

The Issue: The product was potentially exposed to below-recommended storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2022· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...

The Issue: Software related alarm escalation defect occurs after approximately 25 days...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2022· Synapse Biomedical Inc

Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) Recalled by Synapse Biomedical Inc...

The Issue: Firm has revised labeling to consistently call out storage conditions and...

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

Class III — Low RiskOngoing
Medical DeviceMay 31, 2022· Boston Scientific Corporation

Recalled Item: GreenLight HPSEA Laser Fibers Recalled by Boston Scientific Corporation Due...

The Issue: Several complaints were received for the affected lot; users received a...

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

Class III — Low RiskOngoing
Medical DeviceMay 31, 2022· Baxter Healthcare Corporation

Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...

The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2022· Ossur Americas

Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...

The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of...

The Issue: The base of the anesthesia system can have a crack and could potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Paragon 28, Inc.

Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...

The Issue: Due to Titanium plasma coating not present implant.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿...

The Issue: On-Analyzer Stability (OAS) time, supported for 6 weeks; not 8 weeks as is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Olympus Corporation of the Americas

Recalled Item: SOLTIVE SuperPulsed Laser Fibers Recalled by Olympus Corporation of the...

The Issue: Device model and size for affected lots of Laser Fibers may be mismatched...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Absorbent dressings. a. DERMA SCIENCES Recalled by Mckesson Medical-Surgical...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: DERMARITE INDUSTRIES SafeWash Saline Saline Wound Flush SafeWash 7.1 oz....

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. SporView Culture Set SporView Sterilization Biological Indicator Kit...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: DERMARITE INDUSTRIES DermaCol 100 Collagen Powder DermaCol 100 Collagen 1...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Skin markers: a. IZI MEDICAL PRODUCTS LLC Multi-Modality Markers SKIN...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing