Reported Mar 27, 2019 · Terminated

HYDROmorphone HCl 1 mg in 0.9% Sodium Chloride, QS 5 mL Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single…

Advanced Pharma Inc.

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: Advanced Pharma Inc. · 9265 Kirby Dr · Houston, TX · 77054-2520

Is this the product you have?

  • HYDROmorphone HCl 1 mg in 0.9% Sodium Chloride, QS 5 mL Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe
  • NDC
    • 42852-289-67 Avella of Houston 9265 Kirby Dr
    • Houston
    • TX 77054 (877) 794-0404
Lot codes and dates

2 of 2 products · 2 lot codes

Recalled lot codes, grouped by product number
LotsBarcodeLot codes and dates
1203
  • 18 4090 28967S Exp. 4/2/2019
1203
  • 18 6221 28967S Exp. 4/2/2019
Amount recalled
2400 syringes

This recall covers 19 products

The agency filed one notice per product. You are reading one of them; the other 18 are below.

6 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Lack of Assurance of Sterility

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jan 14, 2020 · Data as of Sep 19, 5:05 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.