FDA recall event 97884

Winder Laboratories, LLC recall

1 affected product in this FDA recall event.

FDA event information

Event ID: 97884

This page presents the individual FDA enforcement records that belong to this recall event in a readable format.

The records above are reformatted from openFDA for readability.

FDA recall number: H-0569-2026
Company: Winder Laboratories, LLC
Reason: Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Classification: Class III