inforMED
MalfunctionFMT

GIRAFFE

Received Jun 17, 2026 · Event occurred Mar 25, 2026

Report 3036470679-2026-00078 · MDR key 25534607

Device

Generic name

Warmer, Infant Radiant

Manufacturer

Datex-ohmeda, Inc.

Model number

WARMER

Catalog number

NA

Lot number

NA

Product problems

  • Detachment of Device or Device Component

Patient

Not reported

  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

GE HEALTHCARE (GEHC) REPORTED A FIELD MODIFICATION FOR AN ISSUE THAT CAN DELIVER AN OXYGEN CONCENTRATION THAT DOES NOT MATCH THE INTENDED CONCENTRATION SET BY THE USER PER 21 CFR 806 ON 20-MAY-2026. (GEHC REFERENCE # FMI 32102). CUSTOMERS WERE SENT A LETTER EXPLAINING THE ISSUE AND PROVIDING INSTRUCTIONS FOR INSPECTING FOR DEVICES THAT HAVE AN AFFECTED BLENDER. GEHC WILL REPLACE ALL AFFECTED UNITS. BLOCK A: NO PATIENT INVOLVEMENT. LEGAL MANUFACTURER: GEHC TROUT - 3114 N GRANDVIEW BLVD. USA WAUKESHA, WI 53188.

Description of Event or Problem

THIS UNIT WAS IDENTIFIED AS HAVING AN ISSUE THAT CAN DELIVER AN OXYGEN CONCENTRATION THAT DOES NOT MATCH THE INTENDED CONCENTRATION SET BY THE USER AND MAY BE IMPACTED BY THE ISSUE BEING ADDRESSED AS PART OF CORRECTION AND REMOVAL INITIATED BY GE HEALTHCARE (GEHC) ON 20-MAY-2026 (GEHC REFERENCE # FMI 32102). THERE WAS NO PATIENT INVOLVEMENT.

Remedial action

  • Recall