Metha® MONO NC274TRecalls & reported problems
Aesculap AG · METHA µCAP 12/14 130°/0° SIZE 4 · Class 2 · Implant
Data updated Oct 16, 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 04046963347239), received between Dec 16, 2021 and Dec 16, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Expiration Date Error” (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.
Most reported problems
Device problems
- Expiration Date Error1
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.
MalfunctionDec 16, 2021Expiration Date Error; Expiration Date Error
IT WAS REPORTED TO AESCULAP AG THAT A METHA CAP 12/14 130°/0° SIZE 4. (PART # NC274T) WAS IMPLANTED DURING A TOTAL HIP REPLACEMENT PROCEDURE PERFORMED ON (B)(6) 2021. ACCORDING TO THE COMPLAINANT, FOLLOWING THE PROCEDURE, IT WAS DISCOVERED THAT THE IMPLANT WAS EXPIRED. REPORTEDLY, DURING THE PROCEDURE, THE SALES REPRESENTATIVE CONFIRMED THE SIZE AND EXPIRATION DATE (EXP 11-30-2024) WITH THE CIRCULATOR IN THE ROOM. THE IMPLANTS WERE THEN OPENED AND IMPLANTED. HOWEVER, UPON ENTERING THE USAGE INFORMATION INTO THE DEVICE TRACKING SYSTEM, THE SALES REPRESENTATIVE WAS PROMPTED WITH A WARNING THAT THE PRODUCT WAS EXPIRED. THE COMPLAINT DEVICE HAS NOT BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THE EVENT. ALTHOUGH REQUESTED, ADDITIONAL INFORMATION HAS NOT BEEN MADE AVAILABLE. THE MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13017776 ↗
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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 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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