Motiva® SmoothSilk® Round Ergonomix Breast Implant ERSM-220QRecalls & reported problems
Establishment Labs S.A. · Motiva® SmoothSilk® Round Ergonomix Breast Implant Round Ergonomix Breast Implant - Mini with Qid 220 cc · Class 3 · Implant
All models of Motiva SmoothSilk Round Ergonomix Breast Implant (69)
Data updated Oct 18, 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 07445161011947), received between Oct 3, 2024 and Oct 3, 2024 — classified as 1 injury.
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.
InjuryOct 3, 2024Break; Break
IT WAS REPORTED THAT ULTRASOUND IMAGING SUGGESTED A POSSIBLE COMPROMISE IN THE INTEGRITY OF THE RIGHT IMPLANT. INTRAOPERATIVE FINDINGS LATER CONFIRMED A RUPTURE OF THE RIGHT IMPLANT DURING SURGICAL EXPLORATION. SPECIFIC PATIENT DEMOGRAPHICS, SUCH AS AGE, WEIGHT, AND ETHNICITY, WERE NOT PROVIDED BY THE REPORTER. ADDITIONAL FOLLOW-UPS ARE ONGOING TO GATHER FURTHER INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20364547 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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