Recall company profile

Vortran Medical Technology 1, Inc. Recalls

Overview of recall records associated with Vortran Medical Technology 1, Inc., including dates, categories and classifications where available.

2recall records
May 24, 2017latest record date
May 24, 2017earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceMay 24, 2017

VORTRAN Automatic Resuscitator, VARPlus recall — FDA Z-2091-2017

Vortran received a customer complaint that the spin-nut-DSS connector was assembled in the reverse direction on the oxygen tubing; making the connector unable to be screwed on due to the…

Class IIFDA: TerminatedVortran Medical Technology 1, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Vortran Medical Technology 1, 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.