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Pharma-Natural Inc. 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.

United States

TerminatedClass III

Company
Pharma-Natural Inc.
Product
Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary S…
Recall date
August 15, 2023
Terminated
January 19, 2024
Source
FDA

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets Not published in this source record 204 bottles (102 twin packs)/30 tablets per bottle Lot: PN10686, Exp. Date 01/24

Distribution

  • Puerto Rico

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1615-2023
Event ID
92953
Status
Terminated
Classification
Class III
Company
Pharma-Natural Inc.
Product description
Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets
Quantity
204 bottles (102 twin packs)/30 tablets per bottle
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 the detection limit.
Recall initiation date
August 15, 2023
Report date
October 4, 2023
Classification date
Not published in this source record
Termination date
January 19, 2024
Distribution pattern
Puerto Rico
UPC, lot, and code information
Lot: PN10686, Exp. Date 01/24
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Pharma-Natural Inc.

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Published
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Distribution
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Published
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Distribution
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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.