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PENTAX

HOYA CORPORATION · Model OS-A70 · UDI-DI 04961333169016

PEA Prescription
1
510(k) clearances
609
Adverse events
5
Recalls
12
Facilities

Description

KEYBOARD FOR EPK-I

Recalls

DateFirmReason
2026-09-09Pentax of America IncWarnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.
2025-07-16Pentax of America IncDuring endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observ
2025-01-29Pentax of America IncDuring endoscopic procedures using a combination of the video processor EPK-i8020c and the i20c series video endoscope, the observed image can become reddish or dark (1.8%). Users
2025-01-29Pentax of America IncDuring endoscopic procedures using a combination of the video processor EPK-i8020c and the i20c series video endoscope, the observed image can become reddish or dark (1.8%). Users
2025-01-29Pentax of America IncDuring endoscopic procedures using a combination of the video processor EPK-i8020c and the i20c series video endoscope, the observed image can become reddish or dark (1.8%). Users

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.