MONOMID 1669BRecalls & reported problems
C.P. Medical Corporation · 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 10790986002521), received between Oct 5, 2023 and Oct 5, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
MalfunctionOct 5, 2023Break; Break
A COMPLAINT WAS RECEIVED REGARDING PART NUMBER 1669B LOT 200115-54, SIZE 3/0 BLACK NYLON (NYL BLA SWAGE SUTURE. THE CUSTOMER STATED THAT THE SUTURES HAD NO TENSILE STRENGTH AND WOULD EASILY BREAK JUST BY INSERTING THE SUTURE THROUGH THE SKIN. THE CUSTOMER FURTHER STATED THAT MANY SURGERIES WERE PERFORMED, AND THAT BREAKAGES OCCURRED DURING PROCEDURES. ACCORDING TO THE CUSTOMER, MOST WERE FOR CLOSING OFF INCISIONS. THE PROVIDER MENTIONED SEVERAL PATIENTS INVOLVED, BUT AN ACTUAL COUNT WAS NOT PROVIDED; THERE WERE NO REPORTS OF DELAYS IN THE PROCEDURES GREATER THAN 30 MINUTES. NO FURTHER INFORMATION WAS OBTAINED FROM THE CLINIC.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17878937 ↗
Other Suture, Nonabsorbable, Synthetic, Polyamide devices
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- ETHILON 698GEthicon, LLC · SUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE119 reports
- ETHILON 1696GEthicon, LLC · SUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE118 reports
- Monosof SN-3695Covidien LP · SUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE2 recalls3 reports
- McKesson S661GXMckesson Medical-Surgical Inc. · Suture, Nonabsorbable, Synthetic, Polyamide2 recalls2 reports
- Surgilon 88861919-41Covidien LP · SUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE2 recalls2 reports
- McKesson S931BXMckesson Medical-Surgical Inc. · Suture, Nonabsorbable, Synthetic, Polyamide2 recalls2 reports
- McKesson S697GXMckesson Medical-Surgical Inc. · Suture, Nonabsorbable, Synthetic, Polyamide2 recalls1 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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