Sp-4 — Class III drug recall D-0322-2021
Terminated recall by Washington Homeopathic Products, Inc., reported 2021-04-14, distributed in CO, MD, TX. An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
| Recall number | D-0322-2021 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Washington Homeopathic Products, Inc., Berkeley Springs, WV, United States |
| Recall initiated | 2021-03-18 |
| Classified | 2021-04-05 |
| Reported by FDA | 2021-04-14 |
| Terminated | 2021-05-13 |
| Distributed | CO, MD, TX |
| Quantity | 114 bottles |
| Lot numbers | 24844, 25500, 26310 |
Product
Sp-4, 100 mL solution bottles, Rx only, Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411
Reason for recall
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
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-0322-2021. 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.