Reported Jul 25, 2018 · Terminated
HYDROmorphone 0.2mg/mL. (Hydromorphone HCL (USP) 20 mg, 0.9% Sodium Chloride (USP) QS 100 mL) Volume: 100mL. Single…
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 0.2mg/mL. (Hydromorphone HCL (USP) 20 mg, 0.9%
- Sodium Chloride (USP) QS 100 mL) Volume
100mL. Single dose bag. Advanced Pharma9265 Kirby DrHouston077054 TX. NDC 15082-221-10
- Lot codes and dates
Lot #: 4/26/18 0520 22110PBUD 8/9/20185/14/18 1350 22110PBUD 8/27/2018
- Amount recalled
- 660 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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