Similac Pro-Sensitive (Abbott) – packaging mix-up (2019)
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
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Brand
Abbott Nutrition, Division of Abbott Laboratories
Lot Codes / Batch Numbers
Carton Batch # 06108XK00, Bottle Batch # 02567X800
Products Sold
Carton Batch # 06108XK00; Bottle Batch # 02567X800
Abbott Nutrition, Division of Abbott Laboratories is recalling Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton. due to a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.. 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
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
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
AL, IN, IA, NY, NC, OH, SC, VA, WI
Page updated: Jan 6, 2026