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Alcon Grieshaber 27+ 337.87Recalls & reported problems

Alcon Laboratories, Inc. · 27+® Advanced DSP Backflush Blunt · Class 1

All models of Alcon Grieshaber 27+ (4)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07612717071407), received between Jan 10, 2023 and Jan 10, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (1 report).

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.

Most reported problems

Device problems

  • Loose or Intermittent Connection1
  • Suction Failure1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 10, 2023Loose or Intermittent Connection; Suction Failure; Loose or Intermittent Connection; Suction Failure

    A PHYSICIAN REPORTED THAT AN OPHTHALMIC BACKFLUSH STOPPED WORKING IN THE MIDDLE OF SURGERY DURING EXTRUSION AND TIP WENT INTO ANTERIOR CHAMBER, WHICH SURGEON TOOK OUT WITH THE HELP OF FORCEPS. A FRESH PACK WAS USED TO COMPLETE THE SURGERY WITHOUT ANY PATIENT HARM. PROCEDURE DETAILS HAVE NOT BEEN PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16130881 ↗

Other Cannula, ophthalmic devices

All Cannula, ophthalmic devices →

Sources and updates

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