Home / Recalls / Pharmedium Services, LLC / D-0626-2020

D-0626-2020 Class III Terminated

Recalled by Pharmedium Services, LLC — Lake Forest, IL

FDA drug recall D-0626-2020 was initiated by Pharmedium Services, LLC on Dec 16, 2019 and is designated Class III. Reason for recall: Subpotent Drug The recall status is terminated (terminated Feb 9, 2021). Affected quantity: 864 bags.

Recall Details

Product Type: Drugs
Report Date: Jan 1, 2020
Initiation Date: Dec 16, 2019
Termination Date: Feb 9, 2021
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 864 bags

Product Description

NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

Reason for Recall

Subpotent Drug

Distribution Pattern

Nationwide in the U.S.

Code Information

Lot #s: 193040035S, Exp. 12/29/2019; 193120031S, Exp. 01/08/2020; 193150024S, Exp. 01/09/20; 193180030S, Exp. 01/12/20; 193240028S, Exp. 01/18/20; 193250022S, Exp. 01/19/20.

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0626-2020
openFDA file date: Nov 3, 2026
Loaded by RegDataLab: Nov 4, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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