HYDROmorphone HCl in 0 — Class III drug recall D-0132-2018
Terminated recall by Pharmedium Services, LLC, reported 2018-01-03, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp. Date
| Recall number | D-0132-2018 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2017-09-26 |
| Classified | 2017-12-22 |
| Reported by FDA | 2018-01-03 |
| Terminated | 2020-05-19 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| NDC | 61553-0165-78 |
| Lot numbers | 172410025C |
| Expiration dates | 2017-11-27 |
Product
HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-165-78
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp. Date
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-0132-2018. 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.