Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported July 8, 2015
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.
Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Milestone Scientific, Inc. recalled Milestone Wand STA Handpiece for the delivery of local anesthesia to dental tissue. Mode… - a low-severity action.
Milestone Wand STA Handpiece for the delivery of local anesthesia to dental tissue. Mode… was recalled by Milestone Scientific, Inc. in July 8, 2015. Reason: Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.. Check the official notice for the remedy. Verify recall #Z-1952-2015 with the FDA Devices before acting.
The recall
Milestone Scientific, Inc. issued this low-severity FDA Devices recall-Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument..
- Low
- severity level
- 166K units
- affected scope
- Class III
- classification
- July 8, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1952-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1952-2015) was formally reported on July 8, 2015, with the manufacturer initiating the action on February 11, 2015. It is classified under Low severity (Class III), with a current status of Terminated. Milestone Scientific, Inc. is listed as the recalling firm, operating out of Livingston, NJ. Federal records list the affected scope as 165,850 units, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument. Distribution data in the federal record shows the product reached: Worldwide distribution. US in FL, IL, NY WA and Puerto Rico, Israel, Croatia, Italy, Australia, Germany, Colombia, UK, Sweden, and UAE.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
165,850 units
Related Recalls
6
3 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-1952-2015 |
| Date reported | July 8, 2015 |
| Date initiated | February 11, 2015 |
| Recalling firm | Milestone Scientific, Inc. |
| Firm location | Livingston, NJ |
| Affected scope | 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. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1952-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Milestone Scientific, Inc.. Units affected: 165,850 units.
Why was this product recalled? ▼
Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 8, 2015. Severity: Low. Recall number: Z-1952-2015.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution. US in FL, IL, NY WA and Puerto Rico, Israel, Croatia, Italy, Australia, Germany, Colombia, UK, Sweden, and UAE..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1952-2015) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported July 8, 2015. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.