Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported January 30, 2013
Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4
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.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Cardinal Health recalled Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged… - a moderate-severity action.
Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged… was recalled by Cardinal Health in January 30, 2013. Reason: The firm discovered that the labeling bears an incorrect strength of 9,000 FCC Units per caplet instead of 3,…. Check the official notice for the remedy. Verify recall #F-0916-2013 with the FDA Food before acting.
The recall
Cardinal Health issued this moderate-severity FDA Food recall-The firm discovered that the labeling bears an incorrect strength of 9,000 FCC Units per caplet instead of 3,….
- Moderate
- severity level
- Class II
- classification
- January 30, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0916-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0916-2013) was formally reported on January 30, 2013, with the manufacturer initiating the action on November 13, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Cardinal Health is listed as the recalling firm, operating out of Zanesville, OH. Federal records list the affected scope as 1,140 caplets.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Product was shipped to the following states: NJ & NY. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1,140 caplets
Related Recalls
6
2 from same agency
Product description
Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0916-2013 |
| Date reported | January 30, 2013 |
| Date initiated | November 13, 2012 |
| Recalling firm | Cardinal Health |
| Firm location | Zanesville, OH |
| Affected scope | 1,140 caplets |
| Distribution | Product was shipped to the following states: NJ & NY |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0916-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4. Recalled by Cardinal Health. Units affected: 1,140 caplets.
Why was this product 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 agency issued this recall? ▼
This recall was issued by the FDA Food on January 30, 2013. Severity: Moderate. Recall number: F-0916-2013.
Where was the recalled product distributed? ▼
Distribution: Product was shipped to the following states: NJ & NY.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0916-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Conair Recalls Over One Million Cuisinart Grill Brushes Due… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported January 30, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.