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Use caution Drug recall · FDA · Published May 31, 2024

Washington Homeopathic Recalls Complete 30C/200C Kit Due to Label Mix-Up

Washington Homeopathic Products recalls 11 kits due to labeling errors. Check lot #32093 for Ferrum Phosphoricum vials mislabeled as Ferrum Metallicum.

🇺🇸 FDA recall #D-0618-2024DrugWashington Homeopathic Products ›
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Recalling firmWashington Homeopathic Products, Inc.260 J R Hawvermale Way · Berkeley Springs, WV 25411-6957
✎ GovInfoNow plain-language explainer

What happened, in plain English

Washington Homeopathic Products, Inc. is recalling 11 units of its Complete 30C/200C Homeopathic Kit because some bottles were incorrectly labeled. Specifically, vials containing Ferrum Phosphoricum 200C were mislabeled as Ferrum Metallicum 200C. The company has not yet provided a remedy or return instructions for this recall. Read more at govinfonow.com/recall/32638-washington-homeopathic-recalls-complete-30c-200c-kit-due-to-label.

Source Summary by GovInfoNow · govinfonow.com/recall/32638-washington-homeopathic-recalls-complete-30c-200c-kit-due-to-label · Updated October 9, 2026 · FDA enforcement record: FDA #D-0618-2024

Cite this page

“Washington Homeopathic Recalls Complete 30C/200C Kit Due to Label Mix-Up.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/32638-washington-homeopathic-recalls-complete-30c-200c-kit-due-to-label. Based on FDA recall #D-0618-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0618-2024%22&limit=1).

Why it’s dangerous

The hazard is a labeling error where one homeopathic medicine (Ferrum Phosphoricum) was placed in bottles labeled as another (Ferrum Metallicum). This could lead users to ingest or use the incorrect substance, potentially causing unintended health effects or delaying proper treatment for their condition.

Who’s affected

Consumers who purchased the Complete 30C/200C Homeopathic Kit nationwide in the USA are affected. Individuals relying on the specific homeopathic ingredient Ferrum Phosphoricum are most at risk of taking the wrong medication.

How to tell if you have this one

Check if you have a Complete 30C/200C Homeopathic Kit containing one hundred 1/2 dram vials. Look for UPC 7 40640 64300 6 and lot number 32093 with an expiration date of 8/31/2028.

  • Brand
    Washington Homeopathic Products
  • Product
    Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Your Kit

    Verify if your kit matches the recalled lot number 32093 and UPC 7 40640 64300 6.

  2. Monitor for Updates

    Since no remedy is currently stated, watch for official updates from Washington Homeopathic Products regarding returns or refunds.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: May 31, 202412. FDA classified it Class III: Jul 25, 202423. Published in FDA’s Enforcement Report: Jul 31, 202434. FDA terminated the recall: Sep 18, 202442024
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. 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-0618-2024 (May 31, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0618-2024 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA