Class III — Milestone Scientific, Inc.
| Recalling firm | MILESTONE SCIENTIFIC, INC. |
|---|---|
| Registered facility | MILESTONE SCIENTIFIC, INC. (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument. |
| Product | Milestone Wand STA Handpiece for the delivery of local anesthesia to dental tissue. Model Number STA-5050-305. The Wand STA handpiece is a single use syringe used in conjunction with the CompuDent STA computer controlled dental injection system. |
| Quantity | 165,850 units |
| Distribution | Worldwide distribution. US in FL, IL, NY WA and Puerto Rico, Israel, Croatia, Italy, Australia, Germany, Colombia, UK, Sweden, and UAE. |
| Initiated | 2015-02-11 |
| Classified | 2015-07-01 |
| Terminated | 2016-09-20 |
| Recall number | Z-1952-2015 |
| 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 III recall — Milestone Scientific, Inc. (Z-1952-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70742/
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