Overview of recall records associated with Beevers Manufacturing & Supply, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
Cannulaide recalled May 2008 due to improper seal of the pouch. The improper seal of the Cannulaide's package could potentially affect the device shelf life.
This page summarizes recall records in which the official source identifies Beevers Manufacturing & Supply, 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.
