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HOPKINS 27093AARecalls & reported problems

Karl Storz GmbH & Co. KG · HOPKINS® Telescope 6° · Class 2

All models of HOPKINS (49)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

  1. Jul 23, 2024Class IIOpen, Classified

    Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

    Z-3219-2024 · Root cause: Process design · Recall details · FDA record ↗

Other Cystoscope and accessories, flexible/rigid devices

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page