Medical DeviceNov 13, 2019
TELEFLEX-MORRISVILLE Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use recall — FDA Z-0009-2020
Device vented gas below the stated pressure.
Class IFDA: TerminatedTELEFLEX-MORRISVILLE
Recall history in this database
Classification mix: Class I: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies TELEFLEX-MORRISVILLE as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.