FDA Drug recall D-1262-2014
Sevoflurane, USP (Inhalation Anesthetic), Rx Only, 250 mL Amber Bottle
- FDA Drug
- Class II
- terminated
- Published 2014-05-07
On 2014-05-07 the FDA classified a Class II recall of Sevoflurane, USP (Inhalation Anesthetic), Rx Only, 250 mL Amber Bottle by Piramal Critical Care, citing failed pH Specifications: product was too acidic.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1262-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-07 |
| Published | 2014-05-07 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Piramal Critical Care |
| Distribution | US |
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
Failed pH Specifications: product was too acidic.
Identifiers
| ndc | 66794-015-25 |
|---|---|
| code_info | Lot #: S2611I28 (exp 9/16), S2511I14 (exp 9/16), S2531I16 (exp 9/16), S2721J21 (exp 10/16), S2871K03 (exp 11/16), S288…Lot #: S2611I28 (exp 9/16), S2511I14 (exp 9/16), S2531I16 (exp 9/16), S2721J21 (exp 10/16), S2871K03 (exp 11/16), S2881K03 (exp 11/16), and S2931K07 (exp 11/16). |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1262-2014%22
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