fentaNYL Citrate — Class I drug recall D-723-2016
Terminated recall by Pharmedium Services, LLC, reported 2016-02-24, distributed in CA, CO, IA, OK, PA, VA, WI. Subpotent Drug
| Recall number | D-723-2016 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2015-01-13 |
| Classified | 2016-02-18 |
| Reported by FDA | 2016-02-24 |
| Terminated | 2016-02-22 |
| Distributed | CA, CO, IA, OK, PA, VA, WI |
| Quantity | 180 syringes |
| Reason classes | potency |
| Lot numbers | 15002077M |
| Expiration dates | 2015-04-02 |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-723-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.