PIONEER SURGICAL TECHNOLOGY Streamline MIS Spinal Fixation System Fixed Rod Holder NON recall — FDA Z-2616-2014
The affected fixed rod holders did not allow the instrument to lock down on the spinal rod.
Overview of recall records associated with PIONEER SURGICAL TECHNOLOGY, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
The affected fixed rod holders did not allow the instrument to lock down on the spinal rod.
This page summarizes recall records in which the official source identifies PIONEER SURGICAL TECHNOLOGY, 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.