Robert Busse & Co. Inc. d.b.a. Busse Hospital Safety Deluxe Bone Marrow Biopsy/ Aspiration recall — FDA Z-0543-2018
BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.
Overview of recall records associated with Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables, including dates, categories and classifications where available.
Classification mix: Class II: 1.
BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.
This page summarizes recall records in which the official source identifies Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables 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.