FDAFDA · Food and drugs·Recall number Z-2167-2019
DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient population.
Published August 14, 2019 · Recall initiated: July 1, 2019
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
Potential for sterile packaging to be compromised
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Centurion Medical Products Corporation
- Distributor
- US Nationwide distribution in the states of AZ, CA, FL, GA, IL, KY, MA, MD, MI, NC, NH, NY, OH, SC, TX, TN, VA, WA, WI.
- Lot
- Lot # 2019052190 Exp: 4/30/2021
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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