High flow infusion line for 20, 23, 25 & 27G cannula system 1279.HFRecalls & reported problems
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08717872018546), received between Jun 25, 2018 and Jul 9, 2018 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Collapse” (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
- Collapse1
- Device Operational Issue1
Patient problems
- Eye Injury1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 9, 2018Collapse
DURING SURGERY THE EYE COLLAPSED. PERHAPS THERE IS SOMETHING WRONG WITH THE GRAVITY INPUT SET IN CARTRIDGES.
Patient problems: Eye Injury
MAUDE report 7669803 ↗MalfunctionJun 25, 2018Device Operational Issue; Device Operational Issue
OUR CUSTOMER CLAIMS THE FOLLOWING PROBLEM WITH OUR HIGH FLOW INFUSION LINE 1279.HF, WHICH SLIPS OFF SEVERAL TIMES DURING SURGERY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7634907 ↗
Other Cannula, Trocar, Ophthalmic devices
- UNITY 00380650004680Alcon Laboratories, Inc. · Cannula, Trocar, Ophthalmic1 recall1 report
- MANI Trocar Kit MTK25S TROCAR KIT 25G SMani, Inc. · Cannula, trocar, ophthalmic1 recall0 reports
- ALCON 00380650003591Alcon Laboratories, Inc. · Cannula, Trocar, Ophthalmic1 recall0 reports
- ALCON 00380650004673Alcon Laboratories, Inc. · Cannula, Trocar, Ophthalmic1 recall0 reports
- ALCON 00380650003560Alcon Laboratories, Inc. · Cannula, Trocar, Ophthalmic1 recall0 reports
- ALCON 00380650003584Alcon Laboratories, Inc. · Cannula, Trocar, Ophthalmic1 recall0 reports
- ALCON 00380650003539Alcon Laboratories, Inc. · Cannula, Trocar, Ophthalmic1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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