Reported Mar 23, 2016 · Terminated
NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag,…
Pharmedium Services, LLC
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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: Pharmedium Services, LLC · 150 N Field Dr Ste 350 · Lake Forest, IL · 60045-2506
Is this the product you have?
- NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-134-61
- Lot codes and dates
Service Code 2K613415342084S15342191S15342223S15342224S15342225Sand 15342226Sexp 2/10/201615343025S15343026S15343129Sand 15343131Sexp 2/11/201615344157S15344160Sand 15344209Sexp 2/12/201615345036S15345104S15345106Sand 15345142Sexp 2/13/201615346015S15346016S15346017S15346018S15346019S15346020S15346022Sand 15346023Sexp 2/14/201615348152Sand 15348197Sexp 2/16/2016 15350046Sand 15350154Sexp 2/18/2016
- Amount recalled
- 6,816 bags
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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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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