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FDAFDA · Food and drugs·Recall number Z-0120-2018

Halyard Closed Suction System for Adults, 14 F, Elbow, Directional Tip, Wet Pak. 12 vials per kit, 20 kits per case.

Published November 29, 2017 · Recall initiated: October 6, 2017

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Received recall notification from Smiths Medical that lots of 15ml Saline Vials may be susceptible to leaking and could potentially result in the exposure of the saline contents to infectious agents.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Halyard Health, Inc
Distributor
Distributed domestically to AL, AZ, CA, CO, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, OK, PA, PR, RI, SC, SD, TN, TX, VA, WA, WV
Lot
Product Code 22169, Lots AB6123U08, AB6123U11
Risk classification
Class II
Area (FDA)
device
Country
United States

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