Overview of recall records associated with ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL, including dates, categories and classifications where available.
Classification mix: Class II: 1.
During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX.
This page summarizes recall records in which the official source identifies ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL 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.
