RecallRadar

FDA Device recall Z-1798-2012

Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringe…

On 2012-06-20 the FDA classified a Class II recall of Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringe… by Vygon, citing 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 Loc….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1798-2012
ClassificationClass II
Statusterminated
Initiated2012-05-11
Published2012-06-20
Last updated2026-09-13 11:53 UTC
CompanyVygon
DistributionUS

Product

Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringes are used to maintain the patency of indwelling catheter lumens

Reason

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.

Identifiers

code_info
Product Code VIH-2233 -- lots 87-133-9D, 93-088-9D, 97-066-9D, 00-015-9D, 03-012-9D, 03-113-9D, 03-116-9D, 08-067-9D,…Product Code VIH-2233 -- lots 87-133-9D, 93-088-9D, 97-066-9D, 00-015-9D, 03-012-9D, 03-113-9D, 03-116-9D, 08-067-9D, 08-071-9D, 95-027-9D, 95-029-9D, and 08-073-9D.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1798-2012%22

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