FDA recall record

Washington Homeopathic Products Macula Pellets Homeopathic Medicine, 1 Oz bottles recall — FDA D-0321-2021

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

Class IIIclassification
D-0321-2021official record ID
Apr 14, 2021report date

Recall record at a glance

Official recordD-0321-2021
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmWashington Homeopathic Products, Inc.
Report dateApr 14, 2021
Recall initiation dateMar 18, 2021
Quantity1,909 bottles
LocationBerkeley Springs, WV, United States

Official product description

Macula Pellets Homeopathic Medicine, 1 Oz bottles, Rx only, Manufactured for: Natural Ophthalmics Inc. PO Box 1510 Dillon, CO 80435, NDC 58770-190-42

Why the product was recalled

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

Distribution information

Product was distributed to MD, CO & TX only

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.