Ropivacaine HCl 0 — Class III drug recall D-0934-2017
Terminated recall by Pharmedium Services Llc, reported 2017-07-12, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp Date
| Recall number | D-0934-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services Llc, Lake Forest, IL, United States |
| Recall initiated | 2017-02-15 |
| Classified | 2017-07-02 |
| Reported by FDA | 2017-07-12 |
| Terminated | 2020-01-13 |
| Distributed | Nationwide (US) |
| Quantity | 21 i.v |
| Reason classes | labeling |
| NDC | 61553-0100-13 |
| Lot numbers | 170310113S |
Product
Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13
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-0934-2017. 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.