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High RiskFDAfda-F-1290-2014UNDECLARED ALLERGEN

L-Carnitine, labeled in part as "Healthy Life Chemistry" By Purity First, Est. 1991, packaged in white bottles (90 capsules per bottle) w...

Category
Units Affected
0
Recall Date
September 4, 2013
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1290-2014.

The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1290-2014.

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 Mira Health Products Ltd. 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-1290-2014.

Mira Health Products Ltd.

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 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.

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Mira Health Products Ltd. Recall FAQ

Mira Health Products Ltd. is the subject of a food safety report: L-Carnitine, labeled in part as "Healthy Life Chemistry" By Purity First, Est. 1991, packaged in white bottles (90 capsules per bottle) w.... The notice was published on September 4, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.