Fisher & Paykel Healthcare Inc RT130 and RT131 Neonatal/ Infant Breathing Circuits, heated wire. For use with MR850 Respiratory Humidifier. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
RT130 and RT131 Neonatal/ Infant Breathing Circuits, heated wire. For use with MR850 Respiratory Humidifier.
Brand
Fisher & Paykel Healthcare Inc
Lot Codes / Batch Numbers
Lot umbers in the range 040701 to 041216
Products Sold
Lot umbers in the range 040701 to 041216
Fisher & Paykel Healthcare Inc is recalling RT130 and RT131 Neonatal/ Infant Breathing Circuits, heated wire. For use with MR850 Respiratory Hum due to Pressure elbow may be partly occluded.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Pressure elbow may be partly occluded.
Recommended Action
Per FDA guidance
Recall was initiated on 12/17/2004 at all firm locations and distributors worldwide. The recall letter includes instructions for performing a mitigation until new stock is supplied.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026