Bradshaw Medical Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw recall — FDA Z-1637-2016
A component failure could cause a situation where the applied torque was significantly higher than the calibrated torque setting.
Overview of recall records associated with Bradshaw Medical Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
A component failure could cause a situation where the applied torque was significantly higher than the calibrated torque setting.
This page summarizes recall records in which the official source identifies Bradshaw Medical 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.