Washington Homeopathic Recalls Sp-4 Potassium Phosphate Solution
Washington Homeopathic Products recalls 114 bottles of Sp-4 solution due to incorrect ingredient manufacturing.
Use caution until it’s fixed
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Contact the company
What happened, in plain English
Washington Homeopathic Products, Inc. is recalling 114 bottles of its Rx-only Sp-4 solution because it was manufactured with Potassium Chloride instead of the intended Potassium Phosphate. The affected items were distributed only to Maryland, Colorado, and Texas. No remedy or return instructions are currently listed in the record. Read more at govinfonow.com/recall/36276-washington-homeopathic-recalls-sp-4-potassium-phosphate-solution.
Source Summary by GovInfoNow · govinfonow.com/recall/36276-washington-homeopathic-recalls-sp-4-potassium-phosphate-solution · Updated October 11, 2026 · FDA enforcement record: FDA #D-0322-2021
Cite this page
“Washington Homeopathic Recalls Sp-4 Potassium Phosphate Solution.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/36276-washington-homeopathic-recalls-sp-4-potassium-phosphate-solution. Based on FDA recall #D-0322-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0322-2021%22&limit=1).
Why it’s dangerous
The product contains the wrong active ingredient (Potassium Chloride instead of Potassium Phosphate). This substitution means the medication will not provide the intended therapeutic effect for its prescribed purpose.
Who’s affected
Patients in Maryland, Colorado, and Texas who have been prescribed Sp-4 solution from this manufacturer. The risk applies specifically to those holding lot numbers 24844, 25500, or 26310.
How to tell if you have this one
Check your bottle for the label 'Sp-4', a volume of 100 mL, and an Rx-only designation. Verify the lot number on the packaging against 24844, 25500, or 26310.
- Brand
Washington Homeopathic Products- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Product was distributed to MD, CO & TX only
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0321-2021 | Macula Pellets Homeopathic Medicine, 1 Oz bottles, Rx only, Manufactured for: Natural Ophthalmics Inc. PO Box 1510 Dillon, CO 80435, NDC 58770-190-42; Lot # 27479, exp. date 11/2022 | 1,909 bottles |
| D-0322-2021 | Sp-4, 100 mL solution bottles, Rx only, Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411; Lot # 24844, 25500, 26310 | 114 bottles |
| D-0323-2021 | LCL-2-0191, 5 gallon carboys, Rx only, Manufactured for: LaCore Labs, LLC, by: Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411; Lot # 28506 | 300 liters |
What to do — step by step
Check your bottle details
Verify that your Sp-4 bottle is a 100 mL solution and check the lot number against 24844, 25500, or 26310.
Contact your healthcare provider
Since no remedy is stated in the record, consult your prescriber regarding the incorrect ingredient and next steps for treatment.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “Product was distributed to MD, CO & TX only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado, Maryland, Texas.
Recall timeline
FDA terminated this recall 56 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0322-2021 (March 18, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0322-2021 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.