Medical DeviceJun 1, 2022
TELEFLEX MEDICAL (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile recall — FDA Z-1126-2022
Reports received of torn corrugated breathing tubes.
Class IIFDA: OngoingTELEFLEX MEDICAL Inc.
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceJun 1, 2022
TELEFLEX MEDICAL (1) Teleflex Flex tube, Product #20011, sterile recall — FDA Z-1127-2022
Reports received of torn corrugated breathing tubes.
Class IIFDA: OngoingTELEFLEX MEDICAL Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies TELEFLEX MEDICAL Inc. 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.