Medical DeviceNov 23, 2016
OMNI LIFE SCIENCE OMNIBotics Tracker Kit -Model: RM-10000 The TOTAL KNEE SURGETICS recall — FDA Z-0610-2017
Incorrect lot number on outer kit
Class IIIFDA: TerminatedOMNI LIFE SCIENCE
Recall history in this database
Classification mix: Class III: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies OMNI LIFE SCIENCE 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.