Class II — Alto Development Corp
| Recalling firm | ALTO DEVELOPMENT CORP. |
|---|---|
| Registered facility | ALTO DEVELOPMENT CORP. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility. |
| Product | Surgical punch; sealed pouches packed in punch shelf box Intended for use by trained surgeons to create circular cuts in soft tissue or openings in soft vessel walls during surgical procedures. |
| Quantity | 411,486 units |
| Distribution | Worldwide Distribution - USA Distribution |
| Initiated | 2017-10-23 |
| Classified | 2018-03-01 |
| Terminated | 2019-04-30 |
| Recall number | Z-0813-2018 |
| 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 — Alto Development Corp (Z-0813-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/79274/
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