KETOROLAC Tromethamine Inj — Class II drug recall D-1241-2015
Ongoing recall by Hospira Inc., reported 2015-07-22, distributed nationwide. Crystallization; identified as calcium salt of Ketorolac
| Recall number | D-1241-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2015-06-30 |
| Classified | 2015-07-15 |
| Reported by FDA | 2015-07-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, SG |
| NDC | 00409-3793, 00409-3793-01, 00409-3793-19, 00409-3793-25, 00409-3795, 00409-3795-01, 00409-3795-19, 00409-3795-25, 00409-3795-49, 00409-3796, 00409-3796-01, 00409-3796-19, 00409-3796-25 |
| Lot numbers | 32106DK, 32220DK, 32221DK, 33235DK, 33236DK, 34163DK, 34164DK, 39263DK, 39264DK |
| Expiration dates | 2015-07-01, 2015-08-01, 2015-09-01, 2015-10-01, 2015-11-01, 2016-02-01, 2016-03-01, 2016-06-01, 2016-07-01, 2016-09-01, 2016-10-01 |
Product
KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Forest, IL 60045 --- NDC 0409-3795-01 --- Also labeled under NOVAPLUS label NDC 0409-3795-49
Reason for recall
Crystallization; identified as calcium salt of Ketorolac
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-1241-2015. 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.