Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1856-2025 — 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 Glide

U.S. FDA — Device Enforcement · United States · 2025-04-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1856-2025
Date of alert: 2025-04-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Prismatik Dentalcraft, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 76254798

Reported risk: Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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