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Drug recall · FDA · Published December 31, 2015

Pharmedium Services, LLC recalls NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag,

Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration

🇺🇸 FDA recall #D-0777-2016DrugPharMEDium Services, LLC ›
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Recalling firmPharmedium Services, LLC150 N Field Dr Ste 350 · Lake Forest, IL 60045-2506
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
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Source Page by GovInfoNow · govinfonow.com/recall/43299-pharmedium-services-llc-recalls-norepinephrine-bitartrate-4-mg-16-mcg · Recall date December 31, 2015 · FDA enforcement record: FDA #D-0777-2016

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“Pharmedium Services, LLC recalls NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag,.” GovInfoNow, recall dated December 31, 2015. https://govinfonow.com/recall/43299-pharmedium-services-llc-recalls-norepinephrine-bitartrate-4-mg-16-mcg. Based on FDA recall #D-0777-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0777-2016%22&limit=1).

How to tell if you have this one

  • Brand
    PharMEDium Services, LLC
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class III
  • Status
    Terminated
  • Distribution
    Nationwide
Recall numberProduct, codes & lotsQuantity
D-0777-2016NORepinephrine 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; Service Code 2K6134; 15342084S, 15342191S, 15342223S, 15342224S, 15342225S, and 15342226S, exp 2/10/2016; 15343025S, 15343026S, 15343129S, and 15343131S, exp 2/11/2016; 15344157S, 15344160S, and 15344209S, exp 2/12/2016; 15345036S, 15345104S, 15345106S, and 15345142S, exp 2/13/2016; 15346015S, 15346016S, 15346017S, 15346018S, 15346019S, 15346020S, 15346022S, and 15346023S, exp 2/14/2016; 15348152S, and 15348197S, exp 2/16/2016 15350046S, and 15350154S, exp 2/18/20166,816 bags
D-0778-2016NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61; Service Code 2K6127; 15342123S, exp 2/10/2016 15349071S, exp 2/17/2016 and 15351050S, exp 2/19/2016—
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Contact PharMEDium Services, LLC

We’ve drafted a message you can send PharMEDium Services, LLC to request your refund or repair — edit it as you like.

Subject: Recall D-0777-2016 — PharMEDium Services, LLC Pharmedium Services, LLC recalls NORepinephrine Bitartrate, 4 mg (16 mcg/m

Hello,

I own a Pharmedium Services, LLC recalls NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag, that is covered by recall D-0777-2016 from PharMEDium Services, LLC.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0777-2016 (December 31, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0777-2016 to see it in context.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA