Ketorolac Trom — Class I drug recall D-0867-2020
Terminated recall by RemedyRepack Inc., reported 2020-02-19, distributed in LA, OK. Presence of Particulate Matter: Medication relabeled at facility was recalled by the manufacturer due to small
| Recall number | D-0867-2020 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | RemedyRepack Inc., Indiana, PA, United States |
| Recall initiated | 2019-12-27 |
| Classified | 2020-03-03 |
| Reported by FDA | 2020-02-19 |
| Terminated | 2020-08-18 |
| Distributed | LA, OK |
| Quantity | 75 |
| Reason classes | specification failure |
| NDC | 70518-1239-00 |
| Lot numbers | B0444562-060118, B0537002-112118 |
| Expiration dates | 2020-04, 2020-07 |
Product
Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M. Use, Rx Only, QTY: 1 ml, Repackaged by: RemedyRepack Inc., Indiana, PA 15701 NDC 70518-1239-00
Reason for recall
Presence of Particulate Matter: Medication relabeled at facility was recalled by the manufacturer due to small black particles noticed during routine visual inspection. of retain samples.
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-0867-2020. 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.