Milestone Wand STA Handpiece for the delivery of local anesthesia to… — Class III medical device recall Z-1952-2015
Terminated recall by Milestone Scientific, Inc., reported 2015-07-08, distributed in FL, IL, NY, PR, WA. Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.
| Recall number | Z-1952-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Milestone Scientific, Inc., Livingston, NJ, United States |
| Recall initiated | 2015-02-11 |
| Classified | 2015-07-01 |
| Reported by FDA | 2015-07-08 |
| Terminated | 2016-09-20 |
| Distributed | FL, IL, NY, PR, WA |
| Countries outside the US | AE, AU, CO, DE, GB, HR, IL, IT, SE |
| Quantity | 165,850 units |
| Reason classes | labeling |
| Lot numbers | 140103 |
| Model numbers | STA-5050-305 |
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.
Reason for recall
Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1952-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.