DELTA XTEND 230799923Recalls & reported problems
Depuy (Ireland) · DELTA Xtend HUMERAL 1 BOTTOM TRAY · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295116776), received between Jan 3, 2024 and Jan 3, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
- Peeled/Delaminated1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 3, 2024Break; Peeled/Delaminated; Break; Peeled/Delaminated
THE TRAY HAS A VERY TINY BREAK, AND THIS DO NOT AFFECT ANY FUNCTIONALITY OF THE INSTRUMENTS. ADDITIONAL EVENT INFORMATION: ON A PLASTIC RACK/CONTAINER, THERE IS PRINTED TEXT ATTACHED COMING OUT FROM THE PAPER TABLE OF CONTENTS ON THE BOTTOM (230799923). THAT RACK IS ALSO BROKEN. THERE WERE INSTRUMENTS THAT WERE DIRTY INSIDE, INCLUDING GLEN RESURFACING REAMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18440828 ↗
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- n.a. 39501XKKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501A2Karl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 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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