MalfunctionFZS
INTEGRA® MILTEX®
Received Apr 20, 2026 · Event occurred Mar 19, 2026
Report 24924813 · MDR key 24924813
Device
Generic name
Curette, Surgical, General Use
Manufacturer
Integra Lifesciences Production CorporationModel number
33-53Catalog number
33-53
Lot number
#250402
Patient
0 DA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
3 MM METAL CURETTE REMOVED FROM PACKAGING FOR USE IN DEBRIDEMENT. PRIOR TO USING ON PT, METAL SHARD NOTED TO LOOP FROM MANUFACTURING PROCESS. INSTRUMENT REMOVED FROM USE.