Reported Jul 25, 2018 · Terminated
PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg, 5%Dextrose Inj., USP 250 mL) Volume: 254 mL. Single dose bag.…
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?
- PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg, 5%Dextrose Inj
- USP 250 mL) Volume
254 mL. Single dose bag. Avella of Houston9265 Kirby DrHoustonTX 77054. NDC 42852-893-25
- Lot codes and dates
Lot # 5/23/18 3812 89325PBUD 8/6/2018
- Amount recalled
- 200 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.
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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