Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported June 4, 2025
Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071SRG02660/$$76254798/16D20250219V The Glidewell HT" Implant Twist Drill is indicated to prepare the site for placement of endosseous dental implants when tissue contact will last less than 1 hour. The Glidewell HT" Implant Twist Drill is used to remove bone from osteotomy during dental implant placement. The initial Twist Drill is used to deepen the osteotomy and establish the trajectory of subsequent
Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Prismatik Dentalcraft, Inc. recalled Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071… - a moderate-severity action.
Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071… was recalled by Prismatik Dentalcraft, Inc. in June 4, 2025. Reason: Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device pack…. Check the official notice for the remedy. Verify recall #Z-1856-2025 with the FDA Devices before acting.
The recall
Prismatik Dentalcraft, Inc. issued this moderate-severity FDA Devices recall-Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device pack….
- Moderate
- severity level
- 15 units
- affected scope
- Class II
- classification
- June 4, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1856-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1856-2025) was formally reported on June 4, 2025, with the manufacturer initiating the action on April 14, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Prismatik Dentalcraft, Inc. is listed as the recalling firm, operating out of Irvine, CA. Federal records list the affected scope as 15 units.
The documented reason for this recall is: Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside. Distribution data in the federal record shows the product reached: U.S Nationwide distribution in the states of KY, MA, MI, NC, VA, and WV.. 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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
15 units
Related Recalls
6
3 from same agency
Product description
Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071SRG02660/$$76254798/16D20250219V The Glidewell HT" Implant Twist Drill is indicated to prepare the site for placement of endosseous dental implants when tissue contact will last less than 1 hour. The Glidewell HT" Implant Twist Drill is used to remove bone from osteotomy during dental implant placement. The initial Twist Drill is used to deepen the osteotomy and establish the trajectory of subsequent drills in the placement of a dental implant. The large Twist Drill is stepped to accmmodate the tapered design of the implant and is available in lengths corresponding to the availble implant lengths. Drill length is calculated to indicate where the top of the implant will reside when fully seated to that depth. The Twist Drill is machined from stainless steel.
Reason for recall
Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1856-2025 |
| Date reported | June 4, 2025 |
| Date initiated | April 14, 2025 |
| Recalling firm | Prismatik Dentalcraft, Inc. |
| Firm location | Irvine, CA |
| Affected scope | 15 units |
| Distribution | U.S Nationwide distribution in the states of KY, MA, MI, NC, VA, and WV. |
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-1856-2025) 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? ▼
Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071SRG02660/$$76254798/16D20250219V The Glidewell HT" Implant Twist Drill is indicated to prepare the site for placement of endosseous dental implants when tissue contact will last less than 1 hour. The Glidewell HT" Implant Twist Drill is used to remove bone from osteotomy during dental implant placement. The initial Twist Drill is used to deepen the osteotomy and establish the trajectory of subsequent drills in the placement of a dental implant. The large Twist Drill is stepped to accmmodate the tapered design of the implant and is available in lengths corresponding to the availble implant lengths. Drill length is calculated to indicate where the top of the implant will reside when fully seated to that depth. The Twist Drill is machined from stainless steel.. Recalled by Prismatik Dentalcraft, Inc.. Units affected: 15 units.
Why was this product recalled? ▼
Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 4, 2025. Severity: Moderate. Recall number: Z-1856-2025.
Where was the recalled product distributed? ▼
Distribution: U.S Nationwide distribution in the states of KY, MA, MI, NC, VA, and WV..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1856-2025) 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 June 4, 2025. 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.