Medical DeviceMay 14, 2014
AlloSource AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic recall — FDA Z-1562-2014
The donor was hemodiluted.
Class IIFDA: TerminatedAlloSource, Inc.
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies AlloSource, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.