Myo/Wire II 046-267Recalls & reported problems
A & E Medical Corporation · SS Suture, 3 per sleeve · Class 2 · Implant
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 10841291103790), received between Sep 15, 2025 and Sep 15, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2025Fracture; Fracture
IT WAS REPORTED THAT THE WIRE NEEDLE FRACTURED WHILE BEING PUT THOUGH THE STERNUM. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23051233 ↗
Other Suture, Nonabsorbable devices
- Myo/Wire II 046-367A & E Medical Corporation · Suture, Nonabsorbable4 reports
- Myo/Wire II 040-308A & E Medical Corporation · Suture, Nonabsorbable2 reports
- Myo/Wire II 040-355A & E Medical Corporation · Suture, Nonabsorbable2 reports
- Myo/Wire II 046-093A & E Medical Corporation · Suture, Nonabsorbable1 report
- Myo/Wire II 040-397A & E Medical Corporation · Suture, Nonabsorbable1 report
- Myo/Wire II 046-181A & E Medical Corporation · Suture, Nonabsorbable1 report
- Myo/Wire II 046-062A & E Medical Corporation · Suture, Nonabsorbable1 report
- Myo/Wire II 040-365A & E Medical Corporation · Suture, Nonabsorbable1 report
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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