HOPKINS 27017AARecalls & reported problems
Karl Storz GmbH & Co. KG · HOPKINS® Telescope 0°, 1.9/2.1 mm · Class 2
All models of HOPKINS (49)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04048551073384), received between Oct 29, 2025 and Nov 7, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (3 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Poor Quality Image3
- Device Damaged Prior to Use2
- Chemical Problem1
- Dent in Material1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 7, 2025Poor Quality Image; Device Damaged Prior to Use; Poor Quality Image; Device Damaged Prior to Use
IT WAS REPORTED BLACK DEBRIS WAS COMING OUT OF BOTTOM OF EYE PIECE. FOGGY. NO PATIENT INVOLVEMENT. NO DEATH OR (UNANTICIPATED) SERIOUS DETERIORATION IN STATE OF HEALTH REPORTED
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23501612 ↗MalfunctionOct 29, 2025Poor Quality Image; Dent in Material; Chemical Problem; Material Deformation; Poor Quality Image; Dent in Material; Chemical Problem; Material Deformation
IT HAS BEEN REPORTED THERE WAS BLACK DEBRIS COMING OUT OF BOTTOM OF EYE PIECE. FOGGY. NO PATIENT INVOLVEMENT. NO DEATH OR (UNANTICIPATED) SERIOUS DETERIORATION IN STATE OF HEALTH REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23418086 ↗MalfunctionOct 29, 2025Poor Quality Image; Device Damaged Prior to Use; Poor Quality Image; Device Damaged Prior to Use
IT HAS BEEN REPORTED THERE WAS BLACK DEBRI COMING OUT OF BOTTOM OF EYE PIECE. FOGGY. NO PATIENT INVOLVEMENT. NO DEATH OR (UNANTICIPATED) SERIOUS DETERIORATION IN STATE OF HEALTH REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23418082 ↗
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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.
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