FDA Device recall Z-1952-2015
Milestone Wand STA Handpiece for the delivery of local anesthesia to dental tissue
- FDA Device
- Class III
- terminated
- Published 2015-07-08
On 2015-07-08 the FDA classified a Class III recall of Milestone Wand STA Handpiece for the delivery of local anesthesia to dental tissue by Milestone Scientific, citing wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1952-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-02-11 |
| Published | 2015-07-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Milestone Scientific |
| Distribution | FL, IL, NY, PR, WA |
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
Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.
Identifiers
| code_info | Lot 140103 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1952-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.