PROVIDENCE MEDICAL TECHNOLOGIES Ally Bone Screw - Product Usage:Bone Screws are indicated recall — FDA Z-2428-2020
There may be dimensional manufacturing error that represents a potential safety risk to patients.
Overview of recall records associated with PROVIDENCE MEDICAL TECHNOLOGIES, including dates, categories and classifications where available.
Classification mix: Class II: 1.
There may be dimensional manufacturing error that represents a potential safety risk to patients.
This page summarizes recall records in which the official source identifies PROVIDENCE MEDICAL TECHNOLOGIES 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.