Class II — Musculoskeletal Transplant Foundation, Inc.
| Recalling firm | MUSCULOSKELETAL TRANSPLANT FOUNDATION |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure. |
| Product | QuickGraft® Model # 430PST |
| Quantity | 9 Qty |
| Distribution | NY NC LA TX MO OH |
| Initiated | 2019-08-15 |
| Classified | 2019-09-20 |
| Terminated | 2020-07-01 |
| Recall number | Z-2548-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Musculoskeletal Transplant Foundation, Inc. (Z-2548-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83644/
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