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FoodRecallWatch
Class II, May Cause HarmF-0916-2013

Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4

Recalled by Cardinal Health on Nov 13, 2012

Reviewed by FoodRecallWatch Editorial Team · Updated

Recall Summary

Cardinal Health recalled Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 551 in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Nov 13, 2012.

The FDA-published 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."

The product reached multiple states, recorded by the FDA as "Product was shipped to the following states: NJ & NY." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Zanesville, OH. The recall covers 1,140 caplets of product. The FDA has Terminated this recall (first reported Jan 30, 2013), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.

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.

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

Distribution

Product was shipped to the following states: NJ & NY

What Should You Do?

  • 1.Check your kitchen for this product immediately.
  • 2.Do not consume the recalled product.
  • 3.Return the product to where you bought it for a full refund, or throw it away.
  • 4.If you have experienced any health issues, contact your healthcare provider.

Browse Related Recalls

States affected: New Jersey, New York

Terms Explained

Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.