Genesis BPS, LLC Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx recall — FDA Z-2668-2014
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
Overview of recall records associated with Genesis BPS, LLC., including dates, categories and classifications where available.
Classification mix: Class II: 3.
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
This page summarizes recall records in which the official source identifies Genesis BPS, LLC. 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.