Alcon 8065441720Recalls & reported problems
Alcon Laboratories, Inc. · Microsurgical Instrument HYDRODISSECTION CANNULA 27GA, 11MM BEND · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00380654417202), received between Nov 14, 2022 and Nov 8, 2023 — classified as 4 malfunctions.
The most frequently reported specific device problem is “No Flow” (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.
Reports received per month
Most reported problems
Device problems
- No Flow2
- Blocked Connection1
- Complete Blockage1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 8, 2023No Flow; No Flow
A CUSTOMER REPORTED THAT AN OPHTHALMIC OPERATING CANNULA WAS USED DURING THE SURGERY AND FOUND THAT PROBLEM WITH FLOW. THE SURGERY WAS COMPLETED WITH ALTERNATIVE CANNULA. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18093542 ↗MalfunctionOct 21, 2023Complete Blockage; Complete Blockage
A CUSTOMER REPORTED THAT AN OPHTHALMIC OPERATING CANNULA WAS OBSTRUCTED DURING THE CATARACT SURGERY AND THE SURGERY WAS COMPLETED WITH THE ALTERNATIVE CANNULA. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17981621 ↗MalfunctionJun 5, 2023Blocked Connection; Blocked Connection
A CUSTOMER REPORTED DURING CATARACT SURGERY AN OPHTHALMIC OPERATING SURGICAL CANNULA WAS OBSTRUCTED WITHOUT LUMEN OPENING. PROCEDURE WAS COMPLETED USING ANOTHER CANNULA. THERE WAS NO PATIENT HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17058578 ↗MalfunctionNov 14, 2022No Flow; No Flow
A PHYSICIAN REPORTED THAT DURING A CATARACT SURGERY AN OPHTHALMIC CANNULA CAME AND LIQUID COULD NOT PASS. SURGERY WAS COMPLETED BY ALTERNATE PRODUCT. THERE WAS NO REPORT OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15791714 ↗
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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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