Astra Tech Implant System® 25162Recalls & reported problems
Dentsply Implants Manufacturing GmbH · 1 - Twist Drill EV Ø 1.9, 6-17 mm · Class 1
All models of ASTRA TECH Implant System (166)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07392532146466), received between Feb 2, 2026 and Jun 22, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Fracture” (5 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture5
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 22, 2026Fracture
IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THERE WAS DAMAGE TO THE TOOL HEAD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25580103 ↗MalfunctionJun 22, 2026Fracture
IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THERE WAS DAMAGE TO THE TOOL HEAD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25580058 ↗MalfunctionJun 22, 2026Fracture
IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THERE WAS DAMAGE TO THE TOOL HEAD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25580046 ↗MalfunctionFeb 19, 2026Fracture
TOOL ISSUE - BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24389987 ↗MalfunctionFeb 2, 2026Fracture
CUSTOMER REPORTED A TOOL MALFUNCTION. IT BENT, AND THE PART WHERE IT WAS STUCK ON THE PHONE BROKE. IT GOT STUCK AND COULDN'T BE PULLED OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24242555 ↗
Other Accessories, implant, dental, endosseous devices
- N/A 68015189Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous388 reports
- N/A 68015191Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous319 reports
- N/A 68015193Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous283 reports
- N/A 68015187Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous266 reports
- N/A 68015188Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous185 reports
- N/A 68015192Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous159 reports
- N/A 68015190Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous147 reports
- NobelReplace® 37045Nobel Biocare AB · Accessories, implant, dental, endosseous2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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