Visitec® 585282Recalls & reported problems
Beaver-Visitec International, Inc. · Viscoflow® Cannula .40 x 22mm (27G x 7/8 in) · Class 1
All models of Visitec (3)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30886158003015), received between Apr 28, 2023 and Apr 28, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (3 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.
Most reported problems
Device problems
- Contamination /Decontamination Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 28, 2023Contamination /Decontamination Problem; Contamination /Decontamination Problem
CUSTOMER COMPLAINED OF A COATING FOUND ON THE CANNULA. (1 OF 2).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16840395 ↗MalfunctionApr 28, 2023Contamination /Decontamination Problem; Contamination /Decontamination Problem
CUSTOMER REPORTED THAT "CONTAMINATION AND MISSING EXPIRY DATE HAS BEEN IDENTIFIED WITHIN BATCH DURING INCOMING INSPECTION."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16840391 ↗MalfunctionApr 28, 2023Contamination /Decontamination Problem; Contamination /Decontamination Problem
CUSTOMER COMPLAINED OF A COATING FOUND ON THE CANNULA. (2 OF 2).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16840390 ↗
Other Cannula, Ophthalmic devices
- iTrack Advance iTrack-ADSNova Eye, Inc. · Cannula, Ophthalmic53 reports
- iTrack 250ANova Eye, Inc. · Cannula, Ophthalmic1 recall2 reports
- Vortex Surgical Inc VS0200.25Vortex Surgical, Inc. · Cannula, Ophthalmic1 recall0 reports
- Vortex Surgical Inc VS0275.27Vortex Surgical, Inc. · Cannula, Ophthalmic1 recall0 reports
- Vortex Surgical Inc VS0220.25Vortex Surgical, Inc. · Cannula, Ophthalmic1 recall0 reports
- Visitec® 585278Beaver-Visitec International, Inc. · Cannula, Ophthalmic1 recall0 reports
- Vortex Surgical Inc VS0205.23Vortex Surgical, Inc. · Cannula, Ophthalmic1 recall0 reports
- Vortex Surgical Inc VS0250.25Vortex Surgical, Inc. · Cannula, Ophthalmic1 recall0 reports
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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