FDA Adverse Event Malfunction Summary report: N

E.T. TAPE 11 ENDOTRACH TUBE HOLDER

MDR report key: 20075148 · Received August 27, 2024

Report

Report Number
20075148
Event Type
Malfunction
Date Received
August 27, 2024
Date of Event
March 14, 2024
Report Date
March 26, 2024
Manufacturer
B&B MEDICAL TECHNOLOGIES
Product Code
CBH
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

PRODUCT PACKAGE OUTDATE DOES NOT MATCH INSIDE PACKAGE OF PACKAGE OUTDATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
939888 E.T. TAPE 11 ENDOTRACH TUBE HOLDER DEVICE, FIXATION, TRACHEAL TUBE CBH B&B MEDICAL TECHNOLOGIES 11010 68812

Patients

Seq Age Sex Outcome Treatment
1 123 YR Unknown