CLASS III Food recall · Reported 22 Jul 2020 · FDA Enforcement Report

Similac Pro-Advance Infant Formula with Iron, Milk-Based recalled

Abbott Nutrition, Division of Abbott Laboratories is recalling Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed, distributed in Connecticut, Maryland, New Jersey, New York, Pennsylvania. The recall was initiated on 11 Jun 2020 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesNo lot or expiration date as bottles were not intended for distribution. Batch Numbers: BW3520316 (List Number 64248) and BW0970914 (List Number 66611).
Quantity recalled111 total cases.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1021-2020
FDA event ID
85855
Classification
Class III
Status
Terminated
Recall initiated
11 Jun 2020
FDA classified
10 Jul 2020
Reported
22 Jul 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Baby Formula

Timeline

11 Jun 2020Recall initiated by company
10 Jul 2020Classified by FDA+29 days
22 Jul 2020Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Water filled bottles labeled as Similac Pro-Advance.

Product as listed by the FDA

Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed, 32 FL OZ (1 QT)

Where it was distributed

Products was distributed to the following states: CT, MD, NJ, NY, & PA.

ConnecticutMarylandNew JerseyNew YorkPennsylvania

Questions about this recall

Is Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed recalled?

Yes. Abbott Nutrition, Division of Abbott Laboratories recalled Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed on 11 Jun 2020. The recall is Class III and its status is Terminated. Recall number F-1021-2020.

Why was it recalled?

Water filled bottles labeled as Similac Pro-Advance.

Which lots are affected?

No lot or expiration date as bottles were not intended for distribution. Batch Numbers: BW3520316 (List Number 64248) and BW0970914 (List Number 66611).

Where was it sold?

Products was distributed to the following states: CT, MD, NJ, NY, & PA.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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