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CriticalFDAfda-F-1771-2012SALMONELLA CONTAMINATION

Probitotic Dietary Supplement. : iFlora¿ Kids Multi-Probiotic¿

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
4,747
Recall Date
July 9, 2012
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1771-2012.

On the evening of Friday, July 6, 2012, Ingredion, Inc. (f/k/a Corn Products U.S., Inc.) the supplier of Galactooligosaccharide (GOS), an ingredient included, in iFlora¿ Kids Multi Probiotic, notified our contract manufacturer that two lots of their GOS material supplied for inclusion in our products were being recalled for a suspected salmonella contamination. Although our contract manufacturer

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1771-2012.

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 Nutri-health Supplements Llc. 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-1771-2012.

Nutri-Health Supplements Llc.

FDA

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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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Nutri-health Supplements Llc. Recall FAQ

Nutri-health Supplements Llc. is the subject of a supplements safety report: Probitotic Dietary Supplement. : iFlora¿ Kids Multi-Probiotic¿. The notice was published on July 9, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 4,747 units are potentially affected.