HOPKINS 24941BARecalls & reported problems
Karl Storz GmbH & Co. KG · HOPKINS® Telescope 30°, · Class 2
All models of HOPKINS (49)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04048551083789), received between Dec 2, 2025 and Dec 2, 2025 — classified as 6 injuries.
The most frequently reported specific device problem is “Break” (6 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.
Reports received per month
Most reported problems
Device problems
- Break6
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryDec 2, 2025Break; Break
IT WAS REPORTED THAT "THE TELESCOPE BROKE DURING THE PROCEDURE" SURGERY WAS PROLONGED MORE THAN 60 MIN. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE MDR: 9610617-2025-02218, 9610617-2025-02219, 9610617-2025-02221, 9610617-2025-02222.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23700762 ↗InjuryDec 2, 2025Break; Break
IT WAS REPORTED THAT "THE TELESCOPE BROKE DURING THE PROCEDURE" SURGERY WAS PROLONGED MORE THAN 60 MIN. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE MDR: 9610617-2025-02218, 9610617-2025-02220, 9610617-2025-02221, 9610617-2025-02222.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23700761 ↗InjuryDec 2, 2025Break; Break
IT WAS REPORTED THAT "THE TELESCOPE BROKE DURING THE PROCEDURE" SURGERY WAS PROLONGED MORE THAN 60 MIN. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE MDR: 9610617-2025-02218, 9610617-2025-02219, 9610617-2025-02221, 9610617-2025-02222.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23700760 ↗InjuryDec 2, 2025Break; Break
IT WAS REPORTED THAT "THE TELESCOPE BROKE DURING THE PROCEDURE" SURGERY WAS PROLONGED MORE THAN 60 MIN. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE MDR 9610617-2025-02218, 9610617-2025-02220, 9610617-2025-02221, 9610617-2025-02222.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23700754 ↗InjuryDec 2, 2025Break; Break
IT WAS REPORTED THAT "THE TELESCOPE BROKE DURING THE PROCEDURE" SURGERY WAS PROLONGED MORE THAN 60 MIN. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE MDR 9610617-2025-02219, 9610617-2025-02220, 9610617-2025-02221, 9610617-2025-02222.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23700753 ↗InjuryDec 2, 2025Break; Break
IT WAS REPORTED THAT "THE TELESCOPE BROKE DURING THE PROCEDURE" SURGERY WAS PROLONGED MORE THAN 60 MIN. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE MDR 9610617-2025-02219, 9610617-2025-02220, 9610617-2025-02221, 9610617-2025-02222.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23700752 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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