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PENTAX EC-2990Li (UDI 04961333254316)Recalls & reported problems

Hoya Corporation · PENTAX VIDEO COLONOSCOPE EC-2990i SERIES · Class 2

All models of PENTAX (72)

Data updated Oct 16, 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 04961333254316), received between Mar 3, 2025 and Mar 3, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Optical Obstruction” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K131855, K251256); they may or may not involve this specific model.

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 1 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Optical Obstruction1

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.

  • MalfunctionMar 3, 2025Optical Obstruction; Optical Obstruction

    THE TIME OF EVENT IS UNKNOWN. THERE WAS NO REPORT OF PATIENT HARM. VIDEO IMAGE FAILURE(SHADOW IN IMAGE).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21501544 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K131855, K251256. One submission often covers many models, so check the product and lot details in each record.

  • Z-2449-2021 · Jul 14, 2021 · Open, Classified
    Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models: EG-2790i, EG-1690K, EG-2490K, EG-2790K, EG27-i10; Gastroscope Family # 2- Gastroscopes with a Water Jet Chan
  • Z-2448-2021 · Jul 14, 2021 · Open, Classified
    Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One Instrument Channel and a Water Jet Channel Models: EC-2990Li, EC-3490Li, EC-3890Li, EC-3490TLi, EC-3490LK, EC
  • Z-1267-2020 · Jan 3, 2020 · Terminated
    Pentax Video Colonoscope Model: EC34-i10L
  • Z-1268-2020 · Jan 3, 2020 · Terminated
    Pentax Video Colonoscope Model: EC38-i10L
  • Z-0636-2017 · Aug 15, 2016 · Terminated
    Pentax Video Colonoscope is intended to be used with a PENTAX video processor (including light source), documentation equipment, Monitor, EndoTherapy Device such as a Biopsy Forcep
  • Z-2068-2016 · Apr 6, 2016 · Terminated
    Colonoscope Intended to provide optical visualization of and therapeutic access to the Lower Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, ti

Other Colonoscope and accessories, flexible/rigid devices

All Colonoscope and accessories, flexible/rigid devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page