Frozen Plasma Recalled

The American National Red Cross recalled one unit of PF 24 plasma, citing improper performance of arm prep. The recall was included in the October 18, 2023, US Food and Drug Administration (FDA) Enforcement Report.

The plasma was coded W20322208193200H, and the FDA reported the following distribution pattern: Georgia, Wisconsin, Maine, Kentucky, Indiana, North Carolina, Mississippi, Illinois, Virginia, Maryland, Arkansas, Iowa, Connecticut, Texas, South Carolina, New Jersey, and Massachusetts.

The American National Red Cross initiated the recall on September 26, 2022. On October 11, 2023, the FDA designated the recall Class II. Products affected by Class II recalls may cause temporary or medically reversible adverse health consequences if used. While remote, a possibility of serious harm also exists.

The FDA terminated the recall on October 11, 2023. PF 24 plasma is plasma frozen within 24 hours of phlebotomy. It is classified as a biologic.