FDAFDA · Food and drugs·Recall number Z-1799-2012
Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 5mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringes are used to maintain the patency of indwelling catheter lumens
Published June 20, 2012 · Recall initiated: May 11, 2012
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
Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Vygon Corporation
- Distributor
- Nationwide Distribution including AZ, CA, DE, FL, IL, IN, IA, KS, KY, MD, MA, MI, MN, MO, NJ, NY, OH, PA, UT, VA, WA, WV, and WI.
- Lot
- Product Code VIH-2235 -- lots 86-088-9D, 87-106-9D, 89-080-9D, 90-048-9D, 91-058-9D, 91-059-9D, 91-135-9D, 92-110-9D, 93-062-9D, 93-063-9D, 94-034-9D, 94-044-9D, 95-030-9D, 95-052-9D, 97-051-9D, 97-053-9D, 97-071-9D, and 97-083-9D.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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