Home / Recalls / Pharmedium Services, LLC / D-723-2016

D-723-2016 Class I Terminated

Recalled by Pharmedium Services, LLC — Lake Forest, IL

FDA drug recall D-723-2016 was initiated by Pharmedium Services, LLC on Jan 13, 2015 and is designated Class I. Reason for recall: Subpotent Drug The recall status is terminated (terminated Feb 22, 2016). Affected quantity: 180 syringes.

Recall Details

Product Type: Drugs
Report Date: Feb 24, 2016
Initiation Date: Jan 13, 2015
Termination Date: Feb 22, 2016
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 180 syringes

Product Description

fentaNYL Citrate, Preservative Free, 5 mcg per mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a 3 mL syringe, code 2R3479, PharMEDium.

Reason for Recall

Subpotent Drug

Distribution Pattern

Nine specific hospital pharmacies in VA, IA, WI, CO, CA, PA, and OK.

Code Information

Lot #: 15002077M, Exp 04-02-2015

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-723-2016
openFDA file date: Oct 27, 2026
Loaded by RegDataLab: Oct 29, 2026

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

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