Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 26, 2015 (12 years ago)

Pregestimil ready to use 20 calorie recall

Recalled by Mead Johnson Nutrition · Evansville, IN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Some Pregestimil 20 Calorie Nursette Bottles from batch EV5A6F were inadvertently packaged in Pregestimil 24 Calorie Nursette cartons. The individual Nursette bottles are correctly labeled as 20 Calorie. The carton is the cardboard sleeve wrapped around 6 bottles, the bottle labels and the outer corrugated case all correctly state 20 calorie.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Pregestimil ready to use 20 calorie, 2 oz bottle; 6 bottles per carton; 8 cartons per case

Quantity: 235 cases

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.

Batch # EV5A6F

Where it was sold

Alaska Alabama Arkansas California Colorado Delaware Florida Georgia Iowa Illinois Kentucky Louisiana Massachusetts Maryland Michigan Mississippi North Carolina Nebraska New Hampshire Ohio Oklahoma Pennsylvania South Dakota Texas Utah Virginia Wisconsin West Virginia

FDA's distribution note: Domestic: AK, AL, AR, CA, CO, DE, FL, GA, IA, IL, KY, LA, MA, MD, MI, MS, NC, NE, NH, OH, OK, PA, SD, TX, UT, VA, WI, WV, Foreign: None

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
Mead Johnson Nutrition
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 26, 2015
In FDA report of
May 13, 2015
Terminated
Oct 27, 2015
FDA recall number
F-2170-2015 · event 70850
Official record
FDA enforcement report search