FDA Adverse Event Injury Summary report: N

PANDA IRES WARMER

MDR report key: 11831598 · Received May 17, 2021

Report

Report Number
2112667-2021-01267
Event Type
Injury
Date Received
May 17, 2021
Date of Event
April 20, 2021
Report Date
May 17, 2021
Manufacturer
DATEX-OHMEDA, INC.
Product Code
FMT
PMA / PMN Number
K122267
Removal / Correction Number
SEEH10
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

UNIQUE IDENTIFIER: (B)(4). NO REPORT OF PATIENT INVOLVEMENT. 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.

Description of Event or Problem · 1

AS A RESULT OF AN INSPECTION THAT WAS COMPLETED AS PART OF CORRECTION AND REMOVAL Z-1846-2019 & Z-1847-2019, THIS SYSTEM WAS IDENTIFIED AS HAVING THE BROKEN LATCH AND/OR CRACKED WALL MALFUNCTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
733055 PANDA IRES WARMER WARMER, INFANT RADIANT FMT DATEX-OHMEDA, INC.

Patients

Seq Age Sex Outcome Treatment
1