AlloSource, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1562-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: March 25, 2014

Date Posted: May 14, 2014

Recall Number: Z-1562-2014

Event ID: 67986

Reason for Recall:

The donor was hemodiluted.

Status: Terminated

Product Quantity: 29

Code Information:

Lot numbers 132095-603, 608, 609, 611-618, 622-629, 631-634, and 636-638. Lot numbers 132095-604, 619, and 621.

Distribution Pattern:

Distribution US nationwide, including Michigan and a distributor in Colorado.

Voluntary or Mandated:

Voluntary: Firm initiated