FDA Adverse Event Malfunction Summary report: N

GIRAFFE WARMER

MDR report key: 9528162 · Received December 27, 2019

Report

Report Number
2112667-2019-02735
Event Type
Malfunction
Date Received
December 27, 2019
Date of Event
December 6, 2019
Report Date
December 27, 2019
Manufacturer
DATEX-OHMEDA, INC.
Product Code
FMT
PMA / PMN Number
K122267
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 1

GE HEALTHCARE (GEHC) REPORTED A FIELD MODIFICATION FOR THIS ISSUE PER 21 CFR 806 ON 20 MARCH 2019. THE FDA RECALL NUMBER IS Z-1846-2019 & Z-1847-2019. CUSTOMERS WERE SENT A LETTER EXPLAINING THE ISSUE AND REQUESTING THE CUSTOMER TO INSPECT THE WARMER BEDSIDE PANEL LATCH AREAS. REPLACEMENT OF BROKEN BEDSIDE PANELS WILL BE PROVIDED BY GEHC. A SET OF WARNING LABELS WILL BE SUPPLIED FOR APPLICATION TO THE BEDSIDE PANELS. THESE LABELS WILL WARN THE USER TO NOT USE THE BEDSIDE PANELS FOR MANEUVERING THE WARMER AND INDICATE THE CORRECT METHOD OF MANEUVERING THE WARMER. AN ADDENDUM TO THE OPERATION AND MAINTENANCE MANUAL WILL ALSO BE PROVIDED EMPHASIZING THE NEED TO CHECK AND ENSURE THAT THE BEDSIDE PANELS AND LATCHES ARE NOT CRACKED, BROKEN, OR DAMAGED BEFORE EVERY PATIENT USE. THE ADDENDUM WILL ALSO CONTAIN INSTRUCTIONS TO INCREASE DETECTABILITY OF BROKEN OR CRACKED BEDSIDE PANELS. ON JUNE 14, 2019 A LETTER WAS SENT TO CUSTOMERS PROVIDING AN ADDITIONAL ADDENDUM, LABELS, AND WALL POSTER. GE HEALTHCARE (GEHC) REPORTED A FIELD MODIFICATION FOR THIS ISSUE PER 21 CFR 806 ON 20 MARCH 2019. THE FDA RECALL NUMBER IS Z-1846-2019 & Z-1847-2019.

Description of Event or Problem · 1

THE HOSPITAL REPORTED A BROKEN FRONT BED SIDE PANEL, WHICH COULD CAUSE A PATIENT FALL. THERE WAS NO REPORT OF PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1318672 GIRAFFE WARMER WARMER, INFANT RADIANT FMT DATEX-OHMEDA, INC.

Patients

Seq Age Sex Outcome Treatment
1