VIDEO ADAPTER MODULE (CAMERA) PVK-1070ZRecalls & reported problems
Pentax Of America, Inc. · VIDEO ADAPTER MODULE EPK W/OUT EYEPC (USED) · Class 1
- 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 04961333240364), received between Mar 9, 2022 and Mar 9, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Poor Quality Image” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Poor Quality Image1
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 9, 2022Poor Quality Image; Poor Quality Image
NO "KNOWLEDGEMENT" OF ADVERSE EVENT. REFER TO EXPIRATION DATE AS COMPLAINT NOTIFICATION. CUSTOMER ADVISED: POOR IMAGE QUALITY. THE TIME OF EVENT IS UNKNOWN. THIS EVENT OCCURRED, NO REPORT OF PATIENT HARM. THE DATE OF EVENT IS UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13716707 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.