M/L-10 1122JRecalls & reported problems
Microline Surgical, Inc. · M/L-10 Clip Cartridge, 10 Clips, Disposable · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00811099010470), received between Aug 22, 2018 and Jul 27, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Defective Component” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Defective Component1
- Material Deformation1
- Positioning Failure1
Patient problems
- No Known Impact Or Consequence To Patient1
- Perforation of Vessels1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 27, 2021Defective Component; Defective Component
VESSEL WAS HURT AND BLEEDING OCCURRED BECAUSE THE SURGEON PULLED THE HANDPIECE AS HE THOUGHT THE CLIP WAS SUCCESSFULLY CLIPPED WHICH ACTUALLY WAS NOT.
Patient problems: Perforation of Vessels
MAUDE report 12226120 ↗MalfunctionAug 22, 2018Positioning Failure; Material Deformation; Positioning Failure; Material Deformation
DURING A SURGICAL PROCEDURE, THE SURGEON NOTICED THAT THE CLIPS DID NOT FORM AS THE SHOULD. THE ML-10 CLIP APPLIER RELEASED A DEFORMED SCISSORED CLIP. THE FINAL BLUE CLIP WAS FULLY CRUSHED BUT STUCK TO ONE SIDE OF THE JAW. THE PROCEDURE WAS EXTENDED BY 5 MINS. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7806353 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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