Reported Jan 1, 2020 · Terminated
NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex…
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 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
- Lot codes and dates
Lot #s: 192930039S Exp. 12/18/19192930041S Exp. 12/18/19192940048S Exp. 12/19/19192940049S Exp. 12/19/19192950031S Exp. 12/20/19192950032S Exp. 12/20/19192960039S Exp. 12/22/19192960040S Exp. 12/22/19192960041S Exp. 12/22/19192960042S Exp. 12/22/19192970034S Exp. 12/22/19192970036S Exp. 12/22/19192970037S Exp. 12/22/19192980043S Exp. 12/25/19192980044S Exp. 12/25/19192980045S Exp. 12/25/19193010042S Exp. 12/26/19193020042S Exp. 12/27/19193030039S Exp. 12/28/19193030040S Exp. 12/28/19193030049S Exp. 12/28/19193040045S Exp. 12/29/19193040046S Exp. 12/29/19193040047S Exp. 12/29/19193080040S Exp. 1/2/20193080041S Exp. 1/2/20193080042S Exp. 1/2/20193080043S Exp. 1/2/20193080044S Exp. 1/2/20193090034S Exp. 1/3/20193090035S Exp. 1/3/20193090036S Exp. 1/3/20193100041S Exp. 1/4/20193100042S Exp. 1/4/20193100043S Exp. 1/4/20193120036S Exp. 1/8/20193150028S Exp. 1/9/20193170033S Exp. 1/11/20193170034S Exp. 1/11/20193170035S Exp. 1/11/20193180035S Exp. 1/12/20193190035S Exp. 1/15/20193190038S Exp. 1/15/20193220038S Exp. 1/16/20193230037S Exp. 1/17/20193240029S Exp. 1/18/20193240030S Exp. 1/18/20193240031S Exp. 1/18/20193250028S Exp. 1/19/20193360031S Exp. 1/30/20
- Amount recalled
- 5820 bags
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Subpotent Drug
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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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