Reported Jul 25, 2018 · Terminated
HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg, 0.9% Sodium Chloride (USP) QS 30 mL) Volume: 30mL. Single dose…
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?
- HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg, 0.9%
- Sodium Chloride (USP) QS 30 mL) Volume
30mL. Single dose syringe. Avella of Houston9265 Kirby DrHoustonTX. NDC 42852-222-63
- Lot codes and dates
Lot #: 3/15/18 0954 22263MBUD 6/13/2018
- Amount recalled
- 480 syringes
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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