Reported Jul 25, 2018 · Terminated
NORepiNEPHrine 8 mg (norepinephrine Bitartrate (USP) 8 mg added to 5% Dextrose Inj. (USP) 250 mL. (Concentration 32…
Avella of Deer Valley, Inc. Store 38
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: Avella of Deer Valley, Inc. Store 38 · 24416 N 19th Ave · Phoenix, AZ · 85085-1887
Is this the product you have?
- NORepiNEPHrine 8 mg (norepinephrine Bitartrate (USP) 8 mg added to 5% Dextrose Inj. (USP) 250 mL. (Concentration 32
- mcg/mL) Volume
258 mL. Single dose bag. Avella of Houston9265 Kirby Dr. HoustonTX 77054. NDC 42852-815-25
- Lot codes and dates
Lot #4/23/18 0101 81525P4/23/18 1020 81525PBUD 6/22/20184/30/18 1123 81525P4/30/18 1311 81525PBUD 6/29/20185/1/18 3456 81525PBUD 6/30/20185/8/18 3213 81525PBUD 7/7/2018
- Amount recalled
- 4,280 bags
This recall covers 38 products
The agency filed one notice per product. You are reading one of them; the other 37 are below.
25 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Lack of Assurance of Sterility: Potential leakage of bags.
This product could cause temporary or reversible health problems — stop using it.
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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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