Overview of recall records associated with Devicor Medical Products Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Small patient labels do not match the primary device label. The primary device label accurately identifies the product as 4010-05-08-T4, while the smaller patient label incorrectly…
This page summarizes recall records in which the official source identifies Devicor Medical Products 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.
