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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87547

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 18, 2021
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Washington Homeopathic Products, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 3

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

D-0321-2021
Recall number
D-0321-2021
Initiated
March 18, 2021
Classification
Class III
Status
Terminated
Quantity
1,909 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot # 27479, exp. date 11/2022

Distribution pattern

Product was distributed to MD, CO & TX only

drug · product 2 of 3

Sp-4, 100 mL solution bottles, Rx only, Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411

D-0322-2021
Recall number
D-0322-2021
Initiated
March 18, 2021
Classification
Class III
Status
Terminated
Quantity
114 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot # 24844, 25500, 26310

Distribution pattern

Product was distributed to MD, CO & TX only

drug · product 3 of 3

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

D-0323-2021
Recall number
D-0323-2021
Initiated
March 18, 2021
Classification
Class III
Status
Terminated
Quantity
300 liters

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot # 28506

Distribution pattern

Product was distributed to MD, CO & TX only