Integra® Miltex® 72-30Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Miltex® Matrix Retainer, Tofflemire Junior · Class 1
- 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 10381780414018), received between Apr 17, 2026 and Apr 17, 2026 — 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. How this data works · Data updated Oct 13, 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.
MalfunctionApr 17, 2026Break
A FACILITY REPORTED THAT THE CA-JR TOFFLEMIRE TYPE RET (72-30) MATRIX BAND FELL OUT OF THE RETAINER WHILE IN THE PATIENT'S MOUTH. THERE WAS A SMALL DELAY IN TREATMENT OF APPROXIMATELY 30 MINUTES; HOWEVER, NO PATIENT INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24911575 ↗
Other RETAINER, MATRIX devices
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.