MST/Dewey 0.9mm Mini A1 Bent Ph Tip 45deg PT-30930Recalls & reported problems
Microsurgical Technology, Inc. · Class 2
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 20844685000917), received between Jun 30, 2017 and Jun 30, 2017 — classified as 1 malfunction.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Eye Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 30, 2017Adverse Event Without Identified Device or Use Problem
THE COMPANY DISTRIBUTOR REPORTED THAT THE SURGEON EXPERIENCED DEBRIS IN THE PATIENT'S EYE DURING PHACOEMULSIFICATION. SOME DEBRIS ADHERED TO THE POSTERIOR CAPSULE HOWEVER, THERE WAS NO REPORTED IMPACT TO THE PATIENT AND THE PROCEDURE WAS COMPLETED AS PLANNED.
Patient problems: Eye Injury
MAUDE report 6683269 ↗
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- Constellation, Ultravit, 25+, TotalPlus, EdgePlus 8065751767Alcon Laboratories, Inc. · Unit, phacofragmentation2 recalls302 reports
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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