Reported Jan 22, 2020 · Terminated

QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800

Assurance Infusion

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: Assurance Infusion · 2626 S Loop W Ste 555 · Houston, TX · 77054-2652

Is this the product you have?

  • QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
Lot codes and dates
  • Lots
    • 07012019@30 Exp. 12/28/2019
    • 08052019@13 Exp. 02/01/2020
    • 09252019@15 Exp. 03/23/2020
    • 10292019@12 Exp. 04/26/2020
    • 10092019@6 Exp. 03/04/2020
    • 10162019@12 Exp. 04/13/2020
    • 12042019@31 Exp. 01/18/2020
    • 12162019@35 Exp. 01/30/2020
    • 11262019@37 Exp. 05/24/2020
Amount recalled
190 vials

This recall covers 118 products

The agency filed one notice per product. You are reading one of them; the other 117 are below.

105 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Lack of sterility assurance.

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 drug enforcement) notice

Notice updated Oct 27, 2021 · Data as of Sep 19, 5:52 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.