Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets
Summary
The FDA issued a Class III for Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablet by Pharma-Natural Inc.. Reason: FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets, Lot: PN10686, Exp. Date 01/24), found the biotin content was below.
Details
Source
Food Recall
External ID
F-1615-2023
Action Date
2023-10-04
Status
Terminated
Category
food
Product Description
Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets
Lot/Code Info: Lot: PN10686, Exp. Date 01/24
Quantity Affected: 204 bottles (102 twin packs)/30 tablets per bottle
Reason for Recall
FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets, Lot: PN10686, Exp. Date 01/24), found the biotin content was below the detection limit.
Distribution
Puerto Rico
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-15
Company
Miami Lakes, FL
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 185 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Pharma-Natural Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pharma-Natural Inc. have FDA actions?
This is the only FDA action we have on record for Pharma-Natural Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1615-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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