Mesh|Ex X101866Recalls & reported problems
Exsurco Medical, Inc. · ASM, Cutting Roller C · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810006780192), received between Mar 5, 2026 and Mar 5, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Failure to Cut” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Cut1
- Mechanical Problem1
- Mechanics Altered1
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 5, 2026Mechanical Problem; Failure to Cut; Mechanics Altered
DURING A PROCEDURE ON (B)(6) 2026, IT WAS REPORTED THAT DURING THE SKIN GRAFT MESHING UTILIZING A 3:1 CUTTING ROLLER THERE WERE MANY MISSED CUTS ALONG THE GRAFTS. DUE TO THE AMOUNT OF MISSED CUTS, ANOTHER PIECE OF SKIN HAD TO BE TAKEN FROM THE PATIENT. A PROCEDURE DELAY OF UNKNOWN LENGTH OCCURRED DUE TO RE-CUTTING HOLES MANUALLY AND RETRIEVING MORE SKIN. REPORTED ROLLER: X101866 MESHEX MSH CUTTING ROLLER C SN: (B)(6).
Patient problems: Unspecified Tissue Injury
MAUDE report 24523699 ↗
Other Expander, Surgical, Skin Graft devices
- N/A 00-7701-000-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft521 reports
- N/A 00-7703-015-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft206 reports
- N/A 00-7703-020-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft103 reports
- MeshgraftTM II Tissue Expansion System 00-2195-013-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft1 recall30 reports
- MESHGRAFT™ 00-2195-000-00Zimmer Orthopaedic Surgical Products, Inc. · EXPANDER, SURGICAL, SKIN GRAFT41 reports
- N/A 00-7703-030-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft33 reports
- N/A 00-7703-040-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft27 reports
- MESHGRAFT™ 00-2195-001-00Zimmer Orthopaedic Surgical Products, Inc. · EXPANDER, SURGICAL, SKIN GRAFT25 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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