AlloSource, Inc. Recall: AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicate
AlloSource, Inc. Recall: AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicate is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: AlloSource, Inc.; Product: AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or voi
| Recalling firm | AlloSource, Inc. |
|---|---|
| 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. |
| Reason for recall | The donor was hemodiluted. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Distribution US nationwide, including Michigan and a distributor in Colorado. |
| Recall initiated | 20140325 |
| Recall number | Z-1562-2014 |
| Category | device |
| State | CO |
| Country | United States |
$29/mo
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