Dairy Aid Enzyme Supplement (Cardinal Health) – incorrect strength (2012)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4
Brand
Cardinal Health
Lot Codes / Batch Numbers
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 &, amp, Batch# M743510, Lot # 13973A, Exp Date 7/2013.
Products Sold
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.
Cardinal Health is recalling Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardin due to 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.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
NJ, NY
Page updated: Jan 12, 2026