fentaNYL Citrate — Class I drug recall D-0093-2017
Terminated recall by Pharmedium Services, LLC, reported 2016-10-19, distributed nationwide. Subpotent Drug: confirmed subpotency in one lot of this product that was packaged and stored in syringes.
| Recall number | D-0093-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2015-07-17 |
| Classified | 2016-10-12 |
| Reported by FDA | 2016-10-19 |
| Terminated | 2017-06-23 |
| Distributed | Nationwide (US) |
| Quantity | 500 syringes |
| Reason classes | potency |
| Lot numbers | 15149004M |
| Expiration dates | 2015-08-27 |
Product
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.
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-0093-2017. 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.