Overview of recall records associated with Centerline Biomedical Inc., including dates, categories and classifications where available.
Classification mix: Class I: 1.
Centerline Biomedical has determined that the coating on the guidewires for lot 2404-2005 may delaminate during use of the guidewire.
This page summarizes recall records in which the official source identifies Centerline Biomedical 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.
