PANOVIEW PLUS HD 892107253Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04055207035092), received between Jul 26, 2023 and Jul 26, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Poor Quality Image” (2 reports).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJul 26, 2023Poor Quality Image; Poor Quality Image

  RICHARD WOLF MEDICAL INSTRUMENTS CORPORATION (RWMIC) RECEIVED A MEDWATCH REPORT, MW5118856, REGARDING AN ISSUE WITH A DISCOSCOPE 25° Ø 5.9MM SL 122MM, PART ID: 892107253, SERIAL: (B)(6). THE MEDWATCH REPORT, MW5118856, STATES THAT THE "SCOPE WAS BLURRY DURING A CASE, CAUSING A DELAY IN CASE AND INCREASED ANESTHESIA TIME. STERILIZATION ISSUES RULED OUT (NO LEAKS). CUSTOMER STATED THE SCOPE HAD RECENLY BEEN REPAIRED IN MARCH 2023 FOR SAME ISSUE." ACCORDING TO THE INITIAL REPORTER, THE REPORTED ISSUE CAUSED A 20 MINUTE DELAY IN THE PROCEDURE WHILE THE BACK-UP DEVICE WAS RETRIEVED TO COMPLETE THE SCHEDULED PROCEDURE. THE REPORTER STATED THE DELAY IN THE PROCEDURE RESULTED IN THE PATIENT BEING AT POTENTIAL RISK DUE TO THE INCREASED ANESTHESIA TIME. THERE WAS NO ADDITIONAL TREATMENT OR PROCEDURE NEEDED. THERE IS NO REPORT OF INJURY TO THE PATIENT OR OTHER PERSONNEL AS A RESULT OF THE REPORTED ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17397735 ↗
• InjuryJul 26, 2023Poor Quality Image; Poor Quality Image

  RICHARD WOLF MEDICAL INSTRUMENTS CORPORATION (RWMIC) RECEIVED A MEDWATCH REPORT, MW5118856, REGARDING AN ISSUE WITH A DISCOSCOPE 25° Ø 5.9MM SL 122MM, PART ID: 892107253, SERIAL # (B)(6). THE MEDWATCH REPORT, MW5118856, STATES THAT THE "SCOPE WAS BLURRY DURING A CASE, CAUSING A DELAY IN CASE AND INCREASED ANESTHESIA TIME. STERILIZATION ISSUES RULED OUT (NO LEAKS). CUSTOMER STATED THE SCOPE HAD RECENLY BEEN REPAIRED IN (B)(6) 2023 FOR SAME ISSUE." ACCORDING TO THE INITIAL REPORTER, THE REPORTED ISSUE CAUSED A 20 MINUTE DELAY IN THE PROCEDURE WHILE THE BACK-UP DEVICE WAS RETRIEVED TO COMPLETE THE SCHEDULED PROCEDURE. THE REPORTER STATED THE DELAY IN THE PROCEDURE RESULTED IN THE PATIENT BEING AT POTENTIAL RISK DUE TO THE INCREASED ANESTHESIA TIME. THERE WAS NO ADDITIONAL TREATMENT OR PROCEDURE NEEDED. THERE IS NO REPORT OF INJURY TO THE PATIENT OR OTHER PERSONNEL AS A RESULT OF THE REPORTED ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17397565 ↗