C-QUR MOSAIC 31143Recalls & reported problems
Atrium Medical Corporation · C-QUR Mosaic, 3.5in x 3.5in, (8.9 cm x 8.9 cm) · Class 2 · Implant
All models of C-QUR MOSAIC (8)
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 00650862311433), received between Nov 12, 2022 and Nov 12, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Patient-Device Incompatibility1
Patient problems
- Adhesion(s)1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 12, 2022Patient-Device Incompatibility; Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THIS EVENT IS DEEMED REPORTABLE BASED ON THE ALLEGATIONS IN A LAWSUIT WHICH, WHILE UNSUBSTANTIATED, SUGGEST THAT A REPORTABLE EVENT MAY HAVE OCCURRED DURING USE OF ATRIUM MEDICAL¿S MESH PRODUCT PLAINTIFF ALLEGEDLY EXPERIENCED ADDITIONAL SURGERY, CHRONIC PAIN, ADHESIONS. SINCE THIS IS A LEGAL MATTER, THE CASE HAS BEEN TURNED OVER TO LEGAL COUNSEL AND FURTHER INFORMATION OBTAINED THROUGH INVESTIGATION OR DISCOVERY MAY FALL UNDER THE ATTORNEY/CLIENT AND/OR WORK PRODUCT PRIVILEGE. HOWEVER, ATRIUM WILL SUPPLEMENT THIS REPORT AS APPROPRIATE IF ADDITIONAL INFORMATION COMES TO ITS ATTENTION.
Patient problems: Adhesion(s); Pain
MAUDE report 15785657 ↗
Other Mesh, surgical, non-absorbable, thoracic, chest wall reconstruction devices
- C-QUR MOSAIC 31133Atrium Medical Corporation · Mesh, surgical, non-absorbable, thoracic, chest wall reconstruction4 reports
- C-QUR MOSAIC 31107Atrium Medical Corporation · Mesh, surgical, non-absorbable, thoracic, chest wall reconstruction3 reports
- C-QUR MOSAIC 31106Atrium Medical Corporation · Mesh, surgical, non-absorbable, thoracic, chest wall reconstruction3 reports
- C-QUR MOSAIC 31138Atrium Medical Corporation · Mesh, surgical, non-absorbable, thoracic, chest wall reconstruction1 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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