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Cardinal Health 200, LLC recalls Presource(R) Kits (custom surgical/procedural kits): The standard and custom kits are packed with all of the specific d
Recalled September 13, 2017 · FDA recall Z-3107-2017 · Cardinal Health 200
Hazard
The firm manufactured and distributed Presource(R) kits which contained BD SafetyGlide" 22GA 1¿ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection. · FDA Class II
Units
184,102 kits
Sold at
Worldwide Distribution - US (Nationwide) and Internationally to Canada
Description
The firm manufactured and distributed Presource(R) kits which contained BD SafetyGlide" 22GA 1¿ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection.
Product
Presource(R) Kits (custom surgical/procedural kits): The standard and custom kits are packed with all of the specific disposable class I, II, and II implantable, life-supporting, or life-sustaining devices required by customers for common surgical and other medical procedures
Manufacturer(s)
Cardinal Health 200, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →