Pharma-Natural Inc. recalls Biotin 5000 mcg dietary supplements with low biotin content detected in FDA samples. Consumers should check lot numbers and contact the company for details.
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.
Pharma-Natural Inc. is recalling Biotin 5000 mcg dietary supplements that were found to have insufficient biotin levels by FDA testing. This means the product may not provide the intended nutritional benefit.
FDA testing found the biotin content in these supplements was below the detection limit. This means the product does not contain enough biotin to meet the intended nutritional claims. The issue is related to the product's composition, not safety risks like injury or illness.
People who purchased Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets) with lot number PN10686 and expiration date 01/24 are affected. Those taking biotin supplements for nutritional needs may be impacted.
Check for lot number PN10686 and expiration date 01/24 on the product label. The product is a dietary supplement called Pharma Natural Biotin 5000 mcg Maximum Strength, 30 tablets.
Look for lot number PN10686 and expiration date 01/24 on the product label.
FDA sample analysis found the biotin content was below the detection limit, meaning the product does not contain enough biotin to meet intended nutritional levels.
The recall record does not specify a remedy, so contact Pharma-Natural Inc. directly for guidance.
No, the hazard is related to insufficient biotin content, not physical safety risks.
We’ve drafted a message you can send Pharma-Natural to request your refund or repair — edit it as you like.
Subject: Recall F-1615-2023 — Pharma-Natural Pharma-Natural Hello, I own a Pharma-Natural that is covered by recall F-1615-2023 from Pharma-Natural. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
