Sevoflurane — Class II drug recall D-1262-2014
Terminated recall by Piramal Critical Care, Inc., reported 2014-05-07, distributed nationwide. Failed pH Specifications: product was too acidic.
| Recall number | D-1262-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Piramal Critical Care, Inc., Bethlehem, PA, United States |
| Recall initiated | 2014-04-07 |
| Classified | 2014-04-25 |
| Reported by FDA | 2014-05-07 |
| Terminated | 2014-12-15 |
| Distributed | Nationwide (US) |
| Quantity | 12,600 bottles |
| NDC | 66794-0015, 66794-0015-25 |
| Lot numbers | S2611I28 |
Product
Sevoflurane, USP (Inhalation Anesthetic), Rx Only, 250 mL Amber Bottle. Manufactured By: Piramal Critical Care, 3950 Schelden Circle, Bethlehem, PA 18017. NDC: 66794-015-25.
Reason for recall
Failed pH Specifications: product was too acidic.
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-1262-2014. 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.