Reported Jun 20, 2012 · Terminated

Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 Units per mL, 5mL in a 10mL Flush Syringe, 30 syringes per box, Rx…

Vygon Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Vygon Corporation · 103 A Park Drive · Montgomeryville, PA · 18936-9613

Is this the product you have?

  • Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 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
Lot codes and dates
    • Product Code VIH-3335 -- lots 89-099-9D
    • 89-143-9D
    • 90-093-9D
    • 92-073-9D
    • 92-097-9D
    • 92-124-9D
    • 92-140-9D
    • 92-142-9D
    • 94-009-9D
    • 94-013-9D
    • 94-045-9D
    • 94-140-9D
    • 94-147-9D
    • 95-013-9D
    • 95-014-9D
    • 95-109-9D
    • 96-049-9D
    • 98-010-9D
    • 99-041-9D
    • 00-012-9D
    • 01-036-9D
    • 01-055-9D
    • 02-065-9D
    • 02-067-9D
    • 02-100-9D
    • 07-020-9D
    • 07-031-9D
    • 07-033-9D
    • 07-041-9D
    • 08-037-9D
    • 08-048-9D
    • 09-007-9D
    • 09-009-9D
    • 09-022-9D
    • 10-001-9D
    • 10-012-9D
    • 10-049-9D
    • 10-039-9D
    • 12-022-9D
    • and 12-026-9D

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 11, 2013 · Data as of Sep 19, 5:24 PM UTC

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