FDA Adverse Event Injury Summary report: N

MICROCUFF

MDR report key: 24527659 · Received March 5, 2026

Report

Report Number
1314417-2026-00010
Event Type
Injury
Date Received
March 5, 2026
Date of Event
February 3, 2026
Report Date
May 20, 2026
Manufacturer
AIRLIFE
Product Code
BTR
UDI-DI
10889483564981
PMA / PMN Number
N/A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
EI
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE PRODUCT INVOLVED IN THE REPORT HAS NOT BEEN RETURNED. A REVIEW OF THE DEVICE HISTORY RECORD IS IN-PROGRESS. ALL INFORMATION REASONABLY KNOWN AS OF (B)(6) 2026 HAS BEEN INCLUDED IN THE HEALTH AUTHORITY REPORT. SHOULD ADDITIONAL INFORMATION BE OBTAINED A FOLLOW-UP HEALTH AUTHORITY REPORT WILL BE PROVIDED. THE INFORMATION PROVIDED BY AIRLIFE. REPRESENTS ALL OF THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT/REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO AIRLIFE. AIRLIFE HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE AIRLIFE COMPLAINT DATABASE AND IS IDENTIFIED AS COMPLAINT - (B)(4). THIS INFORMATION IS SUBMITTED PURSUANT TO 21CFR803, IN COMPLIANCE WITH THE MEDICAL DEVICE REPORTING REQUIREMENT AND SHOULD NOT BE CONSIDERED TO BE AN ADMISSION THAT A AIRLIFE PRODUCT IS DEFECTIVE OR CAUSES SERIOUS INJURY.

Description of Event or Problem · 0

IT WAS REPORTED THAT THEY ARE NOTICING A MARKED INCREASE IN THE INCIDENCE OF PRESSURE AREAS IN PATIENT'S NARES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
206789 MICROCUFF MICROCUFF ENDOTRACHEAL TUBE FOR PEDIATRICS/ORAL/NASAL MAGILL, MURPHY EYE/RADIOP BTR AIRLIFE 35111 UNKNOWN 10889483564981

Patients

Seq Age Sex Outcome Treatment
1