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AlloSource, Inc. recalls AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or
Recalled May 14, 2014 · FDA recall Z-1562-2014 · AlloSource
Hazard
The donor was hemodiluted. · FDA Class II
Units
29
Sold at
Distribution US nationwide, including Michigan and a distributor in Colorado.
Description
The donor was hemodiluted.
Product
AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or voids that are not intrinsic to the stability of the bony structure. AlloFuse is indicated to be packed gently into bony gaps in the skeletal system as a bone graft extender.
Manufacturer(s)
AlloSource, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →