Kii® Optical Dual Pack CTR10Recalls & reported problems
Applied Medical Resources Corporation · Laparoscopic Trocar Sleeve/Single Use · Class 2
Data updated Oct 16, 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 00607915124052), received between Dec 30, 2021 and Dec 30, 2021 — 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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Abdominal Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 30, 2021Break; Break
PROCEDURE PERFORMED: UNKNOWN. EVENT DESCRIPTION: TRANSLATION: THE TROCAR BROKE IN THE ABDOMINAL WALL WHEN THE SURGEON INSERTED A FORCEPS INTO IT. PATIENT OR USER IMPACTS: EMERGENCY CONSULTATION FOR ABDOMINAL PAIN ON (B)(6) 2021 THEN RETURN HOME. SEVERITY: CRITICAL. DECLARATION TO THE ANSM: YES. PATIENT STATUS: EMERGENCY CONSULTATION FOR ABDOMINAL PAIN ON (B)(6) 2021 THEN RETURN HOME.
Patient problems: Abdominal Pain
MAUDE report 13122621 ↗
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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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