Reported Jan 22, 2020 · Terminated
QUADMIX FORTE 30MG/4MG/40MCG/400MCG/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 FORTE 30MG/4MG/40MCG/400MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
- Lot codes and dates
- Lots
07222019@10 Exp. 01/18/202006242019@19 Exp. 12/21/201908132019@15 Exp. 02/09/202010292019@22 Exp. 04/26/202011272019@24 Exp. 01/22/202009182019@18 Exp. 03/16/2020
- Lots
- Amount recalled
- 134 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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