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 84018420 of 55,304 recalls

DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection Recalled by Pine...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Tropi-Phen (tropicamide 1% Recalled by Pine Pharmaceuticals, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 1.25 MG/0.05 ML Solution for Injection Recalled by Pine...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Endophth Kit (Vancomycin 1mg/0.1 mL - Ceftazidime 2.25mg/0.1 mL) Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Foscarnet Sodium 2.4mg/0.1 mL solution for injection Recalled by Pine...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Tropi-Phen (Tropicamide 1% phenylephrine HCl 2.5%) ophthalmic solution...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2023· Edge Biologicals Inc

Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...

The Issue: Due to product outer packaging incorrectly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...

The Issue: Unexpected failure of electrical components within the CPI generator.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Stanbio Laboratory, LP

Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...

The Issue: Deterioration in the stability of the Test Strips results in diminished...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...

The Issue: Sterilization failures when devices are sterilized per the Reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...

The Issue: There is a potential for unexpected failure of the electrical components...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
DrugSeptember 29, 2023· Biomic Sciences, LLC dba ION Intelligence of Nature

Recalled Item: ION*Sinus Spray Recalled by Biomic Sciences, LLC dba ION Intelligence of...

The Issue: Microbial contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2023· Biomic Sciences, LLC dba ION Intelligence of Nature

Recalled Item: Restore Sinus Spray Recalled by Biomic Sciences, LLC dba ION Intelligence of...

The Issue: Microbial contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2023· Biomic Sciences, LLC dba ION Intelligence of Nature

Recalled Item: ION* Sinus Support Nasal Spray Recalled by Biomic Sciences, LLC dba ION...

The Issue: Microbial contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO +VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO VISIAN Implantable Collamer Lens .2. Phakic Intraocular lens. Recalled...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Atrium Medical Corporation

Recalled Item: Atrium Firm PVC Thoracic Catheter 36FR Straight Recalled by Atrium Medical...

The Issue: A sterilization nonconformance prematurely aged the product, resulting in an...

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

Class II — Potential Health HazardOngoing