Winder Laboratories recalls grape-flavored chewable multivitamin tablets with subpotent Vitamin D. The product was found deficient during an FDA inspection. Consumers should contact the manufacturer for details.
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Winder Laboratories is recalling grape-flavored chewable multivitamin tablets that were found to have insufficient Vitamin D levels during an FDA inspection. This means the product may not provide the intended nutritional benefit.
The product was found to be subpotent for Vitamin D during an FDA inspection. This means the product may not contain enough Vitamin D to meet the intended nutritional levels. The deficiency could lead to inadequate Vitamin D intake over time.
People who purchased the specific grape-flavored chewable multivitamin tablets with the listed NDC and UPC numbers are affected. Children and adults using these products are at risk of not receiving adequate Vitamin D.
Check for the product name 'Multivitamin with Fluoride Chewable Tablets Grape Flavor' with NDC 75826-169-10 or 75826-171-10. The UPC numbers are 3 15826 16910 2 or 3 15826 17110 5.
Identify the product by checking the NDC numbers (75826-169-10 or 75826-171-10) and UPC numbers (3 15826 16910 2 or 3 15826 17110 5).
The product was found to be subpotent for Vitamin D during an FDA inspection, meaning it may not contain enough Vitamin D to meet the intended nutritional levels.
The recall does not specify a remedy, so contact Winder Laboratories directly for further instructions.
No, the recall is for a nutritional deficiency issue, not a safety hazard that could cause injury.
We’ve drafted a message you can send Winder Laboratories to request your refund or repair — edit it as you like.
Subject: Recall H-0569-2026 — Winder Laboratories Winder Laboratories Hello, I own a Winder Laboratories that is covered by recall H-0569-2026 from Winder Laboratories. 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.
