Succinylcholine Chloride PF Inj — Class III drug recall D-0223-2021
Terminated recall by US Compounding Inc, reported 2021-01-20, distributed nationwide. Labeling: Incorrect or Missing lot and/or expiration date: The lot number and BUD were printed in the incorrec
| Recall number | D-0223-2021 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | US Compounding Inc, Conway, AR, United States |
| Recall initiated | 2020-12-16 |
| Classified | 2021-01-11 |
| Reported by FDA | 2021-01-20 |
| Terminated | 2021-11-05 |
| Distributed | Nationwide (US) |
| Quantity | 1,534 syringes |
| Reason classes | labeling |
| Expiration dates | 2021-02-17 |
Product
Succinylcholine Chloride PF Inj. 200 mg/10 mL, 10 mL single use syringes, Rx only, US Compounding, 1270 Don's Lane, Conway, AR 72032
Reason for recall
Labeling: Incorrect or Missing lot and/or expiration date: The lot number and BUD were printed in the incorrect position on the product label making it illegible.
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-0223-2021. 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.