Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington Homeopathic
Summary
The FDA issued a Class III for Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeo by Washington Homeopathic Products, Inc.. Reason: Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C..
Details
Source
Drug Recall
External ID
D-0618-2024
Action Date
2024-07-31
Status
Terminated
Category
drug
Product Description
Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington Homeopathic Products, Inc., Berkley Springs, WV 25411, UPC 7 40640 64300 6.
Lot/Code Info: lot #: 32093, Exp. 8/31/2028
Quantity Affected: 11 kits
Reason for Recall
Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
Distribution
Nationwide in the USA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-31
Company
Berkeley Springs, WV
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 39 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Washington Homeopathic Products, Inc. has 57 FDA actions in our database, including 57 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Washington Homeopathic Products, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Washington Homeopathic Products, Inc. have FDA actions?
Washington Homeopathic Products, Inc. has 57 FDA actions in our database, including 57 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0618-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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