Reported Jul 28, 2021 · Terminated

ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine…

Mckesson Medical-Surgical Inc. Corporate Office

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: Mckesson Medical-Surgical Inc. Corporate Office · 9954 Maryland Drive · Richmond, VA · 23233

Is this the product you have?

  • ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine convenience kit for the administration of the COVID-19 vaccine
Lot codes and dates
  • All convenience kit lot numbers distributed 5/4/2021 - 5/24/2021
  • containing syringes as followsa) SYRINGE/NDL, 3CC 25GX1 1/2" BD
  • Lot numbers
    • 9252960
    • 0296288
    • 9252961 b) SYRINGE/NDL
    • 3CC 23GX1 1/2" BD
  • Lot Numbers
    • 0324763
    • 0324761
    • 0324766
    • 0324770
    • 1015383
    • 1020431
Amount recalled
53,388 kits

Where it was sold

  • Nationwide

Why it was recalled

Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.

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

Want the full recall guide?

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 Apr 28, 2022 · Data as of Sep 19, 6:22 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.