PlainRecalls
FDA Drug Moderate Class II Terminated

Autologous Serum 20% Eye Drops in 3 mL droppers Assurance Infusion (713) 533-8800

Reported: January 22, 2020 Initiated: December 20, 2019 #D-0663-2020

Product Description

Autologous Serum 20% Eye Drops in 3 mL droppers Assurance Infusion (713) 533-8800

Reason for Recall

Lack of sterility assurance.

Details

Recalling Firm
Assurance Infusion
Units Affected
32 droppers
Distribution
Nationwide within the United States
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
Autologous Serum 20% Eye Drops in 3 mL droppers Assurance Infusion (713) 533-8800. Recalled by Assurance Infusion. Units affected: 32 droppers.
Why was this product recalled?
Lack of sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on January 22, 2020. Severity: Moderate. Recall number: D-0663-2020.