Dietary Supplement Formula ID A200; Packaged in the following configuration: Bulk A200 Nutr Provider Comp Dige capsules (SKU 92132), pa...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0776-2014.
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0776-2014.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact National Enzyme Co or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0776-2014.
National Enzyme Co
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
National Enzyme Co Recall FAQ
National Enzyme Co is the subject of a baby food & formula safety report: Dietary Supplement Formula ID A200; Packaged in the following configuration: Bulk A200 Nutr Provider Comp Dige capsules (SKU 92132), pa.... The notice was published on October 30, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 106,743 units are potentially affected.