Utodelfia Neonatal 17a-oh-progesterone Ki

Autodelfia Neonatal 17a-Oh-Progesterone Kit Recall The Autodelfia Neonatal 17a-Oh-Progesterone Kit, used to test newborn blood samples, is being recalled across Canada due to a Class I defect. This kit is used by healthcare laboratories to screen newborns for a hormone disorder. The recall affects all healthcare facilities and laboratories in Canada that use this product.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-06-07

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/466d5365-27c6-4e0f-a7d4-d4c1a465d7e6