FDA Adverse Event Malfunction Summary report: N

HUDSON NASAL CANNULA CPAP SET, INFANT, SIZE 4

MDR report key: 2061012 · Received March 14, 2011

Report

Report Number
3004365956-2011-00099
Event Type
Malfunction
Date Received
March 14, 2011
Report Date
February 22, 2011
Manufacturer
TELEFLEX MEDICAL
Product Code
BZD
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

DEVICE IS NOT AVAILABLE FOR EVAL BY MFR. THE LOT NUMBER IS UNK, THEREFORE, A DEVICE HISTORY RECORD (DHR) REVIEW COULD NOT BE PERFORMED. IF SAMPLE BECOMES AVAILABLE OR IF ADD'L INFO IS RECEIVED, A F/U REPORT WILL BE SUBMITTED. EVAL, CONCLUSIONS: DEVICE NOT RETURNED. NO EVAL WILL BE PERFORMED.

Description of Event or Problem · 1

THE EVENT IS REPORTED AS: THE ELBOWS ARE CRACKING OR BREAKING WHEN THE CUSTOMER IS TRYING TO PUT THEM IN THE (B)(4) CIRCUIT. ISSUE WAS DISCOVERED PRIOR TO USE ON A PT DURING INSPECTION/FUNCTIONALITY TESTING. NO INJURIES REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HUDSON NASAL CANNULA CPAP SET, INFANT, SIZE 4 INFANT NASAL CANNULA BZD TELEFLEX MEDICAL NA UNK

Patients

Seq Age Sex Outcome Treatment
1