CLASS I Food recall · Reported 24 Dec 2014 · FDA Enforcement Report

Solgar Enhanced Series Abc Dophilus Powder For Infants And Children recalled

Nbty is recalling Solgar Enhanced Series Abc Dophilus Powder For Infants And Children, distributed in 30 states. The recall was initiated on 14 Nov 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot numbers: 074024-01, 074024-01R1 and 074024-02 Expiration Date: 7/31/15

Quantity recalled3,183 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0710-2015
FDA event ID: 69763
Recalling firm: Nbty, Bohemia, NY
Brand: Solgar Enhanced
Classification: Class I
Status: Terminated
Recall initiated: 14 Nov 2014
FDA classified: 12 Dec 2014
Reported: 24 Dec 2014
Type: Voluntary: Firm initiated
Customers notified by: Press Release
Reason category: Other Reasons
Product category: Other

Timeline

14 Nov 2014	Recall initiated by company
12 Dec 2014	Classified by FDA	+28 days
24 Dec 2014	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

NBTY has recalled ABC Dophlius Powder due to the presense of Rhizopus oryzae fungi.

Product as listed by the FDA

SOLGAR ENHANCED SERIES ABC DOPHILUS POWDER FOR INFANTS AND CHILDREN, NET WT. 1.75 oz (50 g), UPC 0 33984 00010 0. Carefully Manufactured by: Solgar, Inc., 500 Willow Tree Road Leonia, NJ 07605 U.S.A.

Where it was distributed

AL, AR, AZ, CA, CT, CO, FL, IA, IL, IN, MI, ME, MO, MA, NC, NE, NY, NJ, NV, OH, OK, PA, PR, UT, TN, TX, VT, KY, WI, WA, United Kingdom and Israel

Alabama Arkansas Arizona California Colorado Connecticut Florida Iowa Illinois Indiana Kentucky Massachusetts Maine Michigan Missouri North Carolina Nebraska New Jersey Nevada New York

Questions about this recall

Why was it recalled?

NBTY has recalled ABC Dophlius Powder due to the presense of Rhizopus oryzae fungi.

Which lots are affected?

Lot numbers: 074024-01, 074024-01R1 and 074024-02 Expiration Date: 7/31/15

Where was it sold?

AL, AR, AZ, CA, CT, CO, FL, IA, IL, IN, MI, ME, MO, MA, NC, NE, NY, NJ, NV, OH, OK, PA, PR, UT, TN, TX, VT, KY, WI, WA, United Kingdom and Israel

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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