Reported Sep 18, 2013 · Terminated

Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill Product ID: 8881570121 Product Usage: Both…

Covidien LLC

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: Covidien LLC · 15 Hampshire Street · Mansfield, MA · 02048-1113

Is this the product you have?

    • Monoject 0.9% Sodium Chloride Flush Syringe
    • 12
  • mL Syringe with 10 mL Fill Product ID8881570121
  • Product UsageBoth 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
Lot codes and dates
  • Lot Numbers13A0084N 13A0094 13B0364 13C0514
Amount recalled
3,235,860 units

This recall covers 9 products

The agency filed one notice per product. You are reading one of them; the other 8 are below.

Where it was sold

  • Nationwide

Why it was recalled

Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 21, 2015 · Data as of Sep 19, 4:44 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.