NA ARDEQT269002ARecalls & reported problems
Maquet Sas · HOR 14 XO · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03700712400989), received between Sep 8, 2023 and Sep 8, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Nov 8, 2023Open, Classified
A potential for a light system to fall in the operating room.
Z-0761-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
Most reported problems
Device problems
- Detachment of Device or Device Component1
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.
MalfunctionSep 8, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17709385 ↗
Other Holder, Camera, Surgical devices
- Maquet Equipment ARDSAT239020AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239007AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239022AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDEQT239016AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDEQT239022AMaquet Sas · Holder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239024AMaquet Sas · Holder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDSAT639005AMaquet Sas · HOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639019AMaquet Sas · HOLDER, CAMERA, SURGICAL1 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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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