Pneumo-Matic 900-200Recalls & reported problems
Coopersurgical, Inc. · 14 Gauge Insufflation Needle · Class 2
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 00888937003666), received between Apr 16, 2020 and Apr 16, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (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.
Most reported problems
Device problems
- Leak/Splash1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 16, 2020Leak/Splash
PER MEDWATCH 5093562 REPORT STATED "PNEOUMO-MATIC INSUFFLATION NEEDLE SLOW TO OBTAIN/MAINTAIN PNEUMOPERITONEUM. LEAKING NEAR THE WHITE PLASTIC AT THE TOP OF THE DEVICE". REF E-COMPLAINT-(B)(4).
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9967242 ↗
Other Pneumoperitoneum Needle devices
- Surgineedle 172015Covidien LP · pneumoperitoneum needle12 reports
- Surgineedle 172016Covidien LP · Pneumoperitoneum Needle4 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.
How reports and recalls are matched · Editorial policy · Report an error on this page