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Alcon, Infiniti, Intrepid 8065752090Recalls & reported problems

Alcon Laboratories, Inc. · Basic Ultrasound · Class 2

All models of Alcon, Infiniti, Intrepid (9)

Data updated Oct 18, 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 18, 2026.

Recalls naming this device

  1. Jun 28, 2023Class IIOpen, Classified

    Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

    Z-2408-2023 · Root cause: Process control · Recall details · FDA record ↗

Other Instrument, vitreous aspiration and cutting, ac-powered devices

All Instrument, vitreous aspiration and cutting, ac-powered devices →

Sources and updates

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