DELTA XTEND 240799936Recalls & reported problems
Depuy (Ireland) · DELTA Xtend GLENOID CASE TOP TRAY R2 · 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 10603295285991), received between Oct 9, 2025 and Oct 9, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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
- Contamination /Decontamination Problem1
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.
MalfunctionOct 9, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem
IT WAS REPORTED THAT THE MODULE WAS OPENED IN THE STERILE UNIT AND STAFF REMOVED THE PLASTIC FROM THE MODULE. THEY OPENED THE CONTAINER AND TOOK OUT ALL LEVELS TO INSPECT THEM BEFORE WASHING THEM IN THE DISHWASHER. THEY FOUND BLOOD AND TISSUE ON 5 PLACES. THEY ALSO FOUND THAT THE CANNULATED PARTS HAD A BLACK COATING INSIDE THEM. THEY REMOVED THE TISSUE PIECES AND WASH THE INSTRUMENTS AND TRAYS IN THE DISHWASHER. THE BLACK COATING REMAINED AFTER THE FIRST WASH. THEY WASHED THESE INSTRUMENTS AGAIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23256011 ↗
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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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