Reported Jul 30, 2014 · Terminated

Oxycodone HCl Oral Concentrate, 20 mg/mL, Rx (C-II) Packaged and labeled as Morphine Sulfate 20 mg/mL, Mfg: Lannett Co.…

Shamrock Medical Solutions Group LLC

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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: Shamrock Medical Solutions Group LLC · 741 Radio Dr · Lewis Center, OH · 43035-7134

Is this the product you have?

  • Oxycodone HCl Oral Concentrate, 20 mg/mL, Rx (C-II) Packaged and labeled as Morphine Sulfate 20 mg/mL
  • MfgLannett Co. Inc
  • Re-Packaged ByShamrock Medical Solutions Lewis Center, Ohio
  • MfrCody Laboratories Inc., Cody, WY NDC 00527-1426-36
Lot codes and dates
  • Lot #: 002HZI
  • Use By7/20/2013
  • NDC00527-1426-36
Amount recalled
55/1 mL/20mg/mL syringe

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

Why it was recalled

Stop using this product now

Labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL actually contained OxyCODONE HCl 20 mg/mL

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated Jul 31, 2014 · Data as of Sep 19, 7:19 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.