Prismatik Dentalcraft, Inc. 2025-06-04 Health serious FDA
Health · FDA · Recall #FDA-Z-1856-2025
Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code:… Recall
Issued June 4, 2025 · Prismatik Dentalcraft, Inc.
In June 2025, Prismatik Dentalcraft, Inc. recalled the Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code:…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside.
What you should do
- 1 Stop using Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Prismatik Dentalcraft, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Prismatik Dentalcraft, Inc.
- Category
- Health
- Recall date
- June 4, 2025
- Units affected
- Not reported
- Sold at
- U.S Nationwide distribution in the states of KY, MA, MI, NC, VA, and WV.
- Recall number
- FDA-Z-1856-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Prismatik Dentalcraft, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.