Ketamine HCl Injection Solution — Class III drug recall D-0648-2021
Terminated recall by Prisma Health Outsourcing Facility, reported 2021-06-23, distributed in SC. Labeling: Incorrect Exp. Date: Incorrect BUD.
| Recall number | D-0648-2021 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Prisma Health Outsourcing Facility, Simpsonville, SC, United States |
| Recall initiated | 2021-06-08 |
| Classified | 2021-07-02 |
| Reported by FDA | 2021-06-23 |
| Terminated | 2021-09-21 |
| Distributed | SC |
| Quantity | 109 syringes |
| Reason classes | labeling |
| NDC | 73463-0100-01 |
| Lot numbers | K10521042, K20521043 |
| Expiration dates | 2021-08-31 |
Product
Ketamine HCl Injection Solution, 10 mg / 2 mL (5 mg/mL), Rx Only, Compounded by Prisma Health Outsourcing Facility 1071 Holland Rd. Suite 2 Simpsonville, SC 29681. NDC: 73463-0100-01
Reason for recall
Labeling: Incorrect Exp. Date: Incorrect BUD.
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-0648-2021. 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.