Skip to main content
High RiskFDAfda-F-0979-2021UNDECLARED ALLERGEN

Vita Aid SynerClear (Vanilla), VA-924. The product is a powder, packaged in a plastic bottle and a white cap, with a net weight of 650g.

Category
Units Affected
3,072
Recall Date
May 25, 2021
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0979-2021.

Undeclared Milk. Products may be contaminated with milk residue.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0979-2021.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Naturo Aid Pharmaceutical Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-0979-2021.

Naturo Aid Pharmaceutical Inc.

FDA

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.

How to report to FDAFile a report at FDA

Naturo Aid Pharmaceutical Inc. Recall FAQ

Naturo Aid Pharmaceutical Inc. is the subject of a food safety report: Vita Aid SynerClear (Vanilla), VA-924. The product is a powder, packaged in a plastic bottle and a white cap, with a net weight of 650g.. The notice was published on May 25, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 3,072 units are potentially affected.