Apparatus, Pneumoperitoneum, Automatic
FDA adverse event reports and recall history for apparatus, pneumoperitoneum, automatic (product code FDP), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 130
- Deaths
- 1
- Injuries
- 11
- Malfunctions
- 117
Reports per year
Source: FDA adverse event reports by year received, 2011–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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Monitor apparatus, pneumoperitoneum, automatic automatically
DeviceWatch monitors available FDA adverse events and recalls. Growth includes event alerts for Death and Injury reports; Compliance Pro adds safety signals for investigation. FDA publication delays and incomplete collection or analysis coverage limit detection; no signal does not establish the absence of a safety concern. AI summaries and signals are provisional and require human review.