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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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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