HYDROmorphone HCl 0 — Class II drug recall D-0854-2018
Terminated recall by PharMEDium Services, LLC, reported 2018-06-20, distributed nationwide. Superpotent and Subpotent
| Recall number | D-0854-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | PharMEDium Services, LLC, Dayton, NJ, United States |
| Recall initiated | 2018-06-05 |
| Classified | 2018-06-08 |
| Reported by FDA | 2018-06-20 |
| Terminated | 2019-02-06 |
| Distributed | Nationwide (US) |
| Quantity | 2,800 syringes |
| Reason classes | potency |
| Lot numbers | 180820005D, 180990007D, 181000020D |
| Expiration dates | 2018-06-21, 2018-07-08, 2018-07-09 |
Product
HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride, 1 mL Total Volume in 3 mL syringe, Rx, PharMEDium Services, LLC, Dayton, NJ
Reason for recall
Superpotent and Subpotent
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-0854-2018. 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.