Reported Jan 22, 2020 · Terminated
HYDROMORPHONE 2MG/ML INJ in 20 mL syringe 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?
- HYDROMORPHONE 2MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Lot codes and dates
- Lots
12112019@1 Exp. 12/20/201912112019@6 Exp. 12/20/201912162019@23 Exp. 12/25/201912172019@7 Exp. 12/26/2019
- Lots
- Amount recalled
- 4 syringes
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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