Washington Homeopathic Products Candida Albicans Recall

Why it was recalled

cGMP deviations

Product description

Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C, 19C, 24C, 25C, 26C, 30C, 200C, 14X, 15X, 16X, 20X, 288X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411

Lot numbers, UPCs & expiration codes

Lot # 17759, 18479, 18133

Where it was sold

Product was distributed USA nationwide.

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-1127-2022
Classification: Class II
Status: Terminated
Recall initiated: May 13, 2022
FDA report date: Jun 22, 2022
Quantity: 1,047 glass amber bottles
Recall type: Voluntary: Firm initiated
Recalling firm: Washington Homeopathic Products, Inc.

Original FDA data

Every field from FDA enforcement report D-1127-2022, exactly as published.

Show all FDA fields

City: Berkeley Springs
State: WV
Status: Terminated
Country: United States
Event ID: 90202
Address: 260 J R Hawvermale Way
Code information: Lot # 17759, 18479, 18133
Postal code: 25411-6957
Report date: Jun 22, 2022
Product type: Drugs
Recall number: D-1127-2022
Classification: Class II
Recalling firm: Washington Homeopathic Products, Inc.
Product quantity: 1,047 glass amber bottles
Termination date: May 25, 2023
Reason for recall: cGMP deviations
Voluntary / mandated: Voluntary: Firm initiated
Product description: Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C, 19C, 24C, 25C, 26C, 30C, 200C, 14X, 15X, 16X, 20X, 288X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Distribution pattern: Product was distributed USA nationwide.
Recall initiation date: May 13, 2022
Initial firm notification: Letter
Center classification date: Jun 10, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1127-2022, published Jun 22, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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