Medical Device Anterior Capsule Retractor MCR-0001Recalls & reported problems
Microsurgical Technology, Inc. · Class 1
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 20844685004571), received between Jul 7, 2021 and Jul 7, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult to Remove” (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
- Difficult to Remove1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 7, 2021Difficult to Remove
THE SURGEON REPORTED THAT A CTR WAS THREADED THROUGH THE LOOP ON THE CAPSULE RETRACTOR. HE WAS UNABLE TO REMOVE THE CTR FROM THE LOOP AND CUT DOWN THE CAPSULE RETRACTOR AS MUCH AS POSSIBLE AND LEFT IT IN THE BAG.
Patient problems: Insufficient Information
MAUDE report 12128379 ↗
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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