Zevex MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with recall — FDA Z-0698-2018
Particulate found on the Curlin spike.
Overview of recall records associated with Zevex Incorporated (dba Moog Medical Medical Devices Group), including dates, categories and classifications where available.
Classification mix: Class II: 6.
Particulate found on the Curlin spike.
Particulate found on the Curlin spike.
Particulate found on the Curlin spike.
Particulate found on the Curlin spike.
Particulate found on the Curlin spike.
Particulate found on the Curlin spike.
This page summarizes recall records in which the official source identifies Zevex Incorporated (dba Moog Medical Medical Devices Group) 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.