D-724-2016 Class I Terminated

Recalled by Pharmedium Services, LLC — Lake Forest, IL

FDA drug recall D-724-2016 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: 500 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
500 syringes

Product Description

fentaNYL Citrate, Preservative Free, 10 mcg per 1 mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a 3 mL syringe, code 2R3174, PharMEDium

Reason for Recall

Subpotent Drug

Distribution Pattern

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

Code Information

Lot #: 15002250M, 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-724-2016
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.