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WhoMadeMyFood

FDA recall record

Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.

Recall F-2153-2019Class IITerminatedAugust 16, 2019

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of December 4, 2019. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.

Reason

a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.

Code information listed by FDA

Carton Batch # 06108XK00; Bottle Batch # 02567X800

Distribution and firm information

Recalling firm listed by FDA: Abbott Nutrition, Division of Abbott Laboratories

Firm location listed by FDA: Columbus, OH, United States

Distribution reported by FDA: Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin

Product quantity listed by FDA: 13440 cartons but only 550 cartons (6600 bottles) affected

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.