Similac Pro-Advance Infant Formula with Iron
Reason Water filled bottles labeled as Similac Pro-Advance.
Similac Pro-Sensitive recall
Recalled by Abbott Nutrition, Division of Abbott Laboratories · Columbus, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Quantity: 13440 cartons but only 550 cartons (6600 bottles) affected
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Carton Batch # 06108XK00; Bottle Batch # 02567X800
Where it was sold
Alabama Iowa North Carolina New York Ohio South Carolina Virginia Wisconsin
FDA's distribution note: Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Abbott Nutrition, Division of Abbott Laboratories
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 16, 2019
- In FDA report of
- Sep 18, 2019
- Terminated
- Dec 4, 2019
- FDA recall number
- F-2153-2019 · event 83608
- Official record
- FDA enforcement report search