F&P NEOPUFF
Received Mar 19, 2026
Report 9611451-2026-01013 · MDR key 24646463
Device
Generic name
Neopuff Infant Resuscitator
Manufacturer
Fisher & Paykel Healthcare LtdModel number
RD900ALUCatalog number
RD900ALU
Lot number
141126
Product problems
- Break
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Additional Manufacturer Narrative
(B)(4). SECTION G4: THE RD900ALU NEOPUFF INFANT RESUSCITATOR IS NOT SOLD IN THE UNITED STATES OF AMERICA (USA) BUT INSTEAD A SIMILAR PRODUCT, RD900AEU NEOPUFF INFANT RESUSCITATOR IS SOLD IN THE USA. THEREFORE, THE 510(K) NUMBER FOR RD900AEU IS K971695. FISHER & PAYKEL HEALTHCARE (F&P) IS CURRENTLY IN THE PROCESS OF COMPLETING OUR INVESTIGATION. WE WILL PROVIDE A FOLLOW UP REPORT UPON COMPLETION OF OUR INVESTIGATION.
Description of Event or Problem
A HEALTHCARE FACILITY IN ITALY REPORTED VIA A FISHER AND PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE THAT THE GAS OUTLET PORT OF A RD900ALU NEOPUFF INFANT RESUSCITATOR IS BROKEN. THERE WAS NO REPORTED PATIENT CONSEQUENCE.