FDA recall record

Del Mar Reynolds Medical Spacelabs Pediatric Flow Sensor Kit, PN: 376-0561-00 recall — FDA Z-1458-2015

Reports of inaccurate low flow readings. Monitored inspiratory tidal volume (VTi) and expiratory tidal volume (Vte) measurements from the pediatric flow…

Class IIclassification
Z-1458-2015official record ID
Apr 29, 2015report date

Recall record at a glance

Official recordZ-1458-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDel Mar Reynolds Medical, Ltd.
Report dateApr 29, 2015
Recall initiation dateMar 5, 2015
Quantity1040 units total (398 in the US and 642 international)
LocationHertford, United Kingdom

Official product description

Spacelabs Pediatric Flow Sensor Kit, PN: 376-0561-00. This kit is for Spacelabs Healthcare Blease 700/900 Series Ventilators. Designed specifically for the mechanical ventilation of adult and pediatric patients under general anesthesia.

Why the product was recalled

Reports of inaccurate low flow readings. Monitored inspiratory tidal volume (VTi) and expiratory tidal volume (Vte) measurements from the pediatric flow sensor are reporting out of specification low compared to the actual delivered volumes being administered to the patient.

Distribution information

Worldwide Distribution-US including the states of Louisiana, North Carolina, and Washington and the countries of Argentina, Brazil, China, Colombia, Ecuador, Finland, Great Britain, India, Libya, Mexico, Nicaragua, Oman, Philippines, Saudi Arabia, Slovakia, Sri Lanka, United Arab Emirates, and Vietnam.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

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