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
Reported: September 13, 2017 Initiated: August 1, 2017 #Z-3107-2017
Product Description
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
Reason for Recall
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.
Details
- Recalling Firm
- Cardinal Health 200, LLC
- Units Affected
- 184,102 kits
- Distribution
- Worldwide Distribution - US (Nationwide) and Internationally to Canada
- Location
- Waukegan, IL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Cardinal Health 200, LLC. Units affected: 184,102 kits.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 13, 2017. Severity: Moderate. Recall number: Z-3107-2017.
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