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DELTA XTEND 2317-70-017Recalls & reported problems

Depuy (Ireland) · DELTA XTEND Central Screw Metaglene depth gauge · Class 1

All models of DELTA XTEND (194)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295532613), received between Jan 18, 2023 and Jan 19, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Mechanical Jam” (2 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 16, 2026.

Most reported problems

Device problems

  • Mechanical Jam2
  • Break1
  • No Apparent Adverse Event1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 19, 2023Mechanical Jam; No Apparent Adverse Event; Mechanical Jam; No Apparent Adverse Event

    IT WAS REPORTED THAT THE SLIDING DEPTH GAUGE WOULD NOT SLIDE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16206769 ↗
  • MalfunctionJan 18, 2023Break; Mechanical Jam; Break; Mechanical Jam

    IT WAS REPORTED ONE OF THE INSTRUMENTS FROM A BRAND NEW SETS ISN'T WORKING PROPERLY. THE SLIDING DEPTH GAUGE WON'T SLIDE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16199427 ↗

Other GAUGE, DEPTH devices

All GAUGE, DEPTH devices →

Sources and updates

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