Home / Recalls / Pharmedium Services, LLC / D-0093-2017

D-0093-2017 Class I Terminated

Recalled by Pharmedium Services, LLC — Lake Forest, IL

FDA drug recall D-0093-2017 was initiated by Pharmedium Services, LLC on Jul 17, 2015 and is designated Class I. Reason for recall: Subpotent Drug: confirmed subpotency in one lot of this product that was packaged and stored in syringes. The recall status is terminated (terminated Jun 23, 2017). Affected quantity: 500 syringes.

Recall Details

Product Type: Drugs
Report Date: Oct 19, 2016
Initiation Date: Jul 17, 2015
Termination Date: Jun 23, 2017
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 500 syringes

Product Description

fentaNYL Citrate, 10 mcg per 1 mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3174.

Reason for Recall

Subpotent Drug: confirmed subpotency in one lot of this product that was packaged and stored in syringes.

Distribution Pattern

Nationwide

Code Information

Lot Number: 15149004M, Exp 08/27/15

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0093-2017
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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