CLASS II Food recall · Reported 30 Jan 2013 · FDA Enforcement Report
Dairy Aid Lactase Enzyme Supplement, Caplet recalled by Cardinal Health
Cardinal Health is recalling Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, distributed in New Jersey, New York. The recall was initiated on 13 Nov 2012 and the FDA has classified it as Class II.
Check your package
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-0916-2013
- FDA event ID
- 63955
- Recalling firm
- Cardinal Health, Zanesville, OH
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 13 Nov 2012
- FDA classified
- 23 Jan 2013
- Reported
- 30 Jan 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Product category
- Dietary Supplements
Timeline
| 13 Nov 2012 | Recall initiated by company | |
| 23 Jan 2013 | Classified by FDA | +71 days |
| 30 Jan 2013 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The firm discovered that the labeling bears an incorrect strength of 9,000 FCC Units per caplet instead of 3,000 FCC units per caplet.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4
Where it was distributed
Product was shipped to the following states: NJ & NY
Questions about this recall
Why was it recalled?
The firm discovered that the labeling bears an incorrect strength of 9,000 FCC Units per caplet instead of 3,000 FCC units per caplet.
Which lots are affected?
White, oblong caplet, imprinted RP143; Batch# M675030, Lot # 10627AA, Exp Date 11/2012; Batch# M679370, Lot # 10627BA, Exp Date 12/2012; Batch# M675020, Lot # 10627A, Exp Date 11/2012; Batch# M679360, Lot # 10627B, Exp Date 12/2012; Batch# M707960, Lot # 10627C, Exp Date 3/2013; Batch# M712800, Lot # 11469A, Exp Date 3/2013; Batch# M740490, Lot # 11464B, Exp Date 6/2013 & Batch# M743510, Lot # 13973A, Exp Date 7/2013.
Where was it sold?
Product was shipped to the following states: NJ & NY
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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