Potassium Chloride For Injection Concentrate syringe 40 mEq/20 mL — Class II drug recall D-0919-2018
Terminated recall by Medi-Fare Drug and Home Health Center, reported 2018-07-18, distributed in TX. CGMP Deviations: Syringes were filled with 19mL of potassium chloride when the labels displayed a fill of 20mL
| Recall number | D-0919-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medi-Fare Drug and Home Health Center, Blacksburg, SC, United States |
| Recall initiated | 2018-07-03 |
| Classified | 2018-07-12 |
| Reported by FDA | 2018-07-18 |
| Terminated | 2019-04-03 |
| Distributed | TX |
| Quantity | 1,116 syringes |
| Reason classes | labeling, cgmp |
| Expiration dates | 2018-08-20 |
Product
Potassium Chloride For Injection Concentrate syringe 40 mEq/20 mL (2 mEq/mL), Rx only, Medi-Fare Drug Pharmaceutical Compounding 300 West Pine St., Blacksburg, SC 29702 800-622-0007
Reason for recall
CGMP Deviations: Syringes were filled with 19mL of potassium chloride when the labels displayed a fill of 20mL.
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-0919-2018. 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.