McKesson 25-2691Recalls & reported problems
Mckesson Medical-Surgical Inc. · LACERATION TRAY, NW TWL · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10612479182339), received between Feb 25, 2025 and Feb 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination” (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.
Reports received per month
Most reported problems
Device problems
- Contamination1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 25, 2025Contamination; Contamination
THE SCISSOR IN THIS KIT WAS FOUND TO BE RUSTY. ON 02/10/24, THE CUSTOMER REPORTED THE CLINIC HAD RUST FALL FROM BRAND NEW IRIS SCISSORS ON STERILE FIELD. THE CUSTOMER STATED THE SCISSORS WAS NOT USED WHEN ASKED IF DETECTED BEFORE USE. CUSTOMER CONFIRMED THE RUST FELL ON THE STERILE FIELD ONLY. NO RUST FELL INTO THE PATIENT'S WOUND/SURGICAL SITE. THE WAS A 15-MINUTE DELAY TO SET UP A NEW STERILE FIELD.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 21459376 ↗
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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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