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Abbott Nutrition, Division of Abbott Laboratories Recall: Water filled bottles labeled as Similac Pro-Advance.

United States

TerminatedClass III

Company
Abbott Nutrition, Division of Abbott Laboratories
Product
Similac Pro-Advance Infant Formula with Iron, Milk-Based, Re…
Recall date
June 11, 2020
Terminated
November 6, 2020
Source
FDA

Reason for recall

Water filled bottles labeled as Similac Pro-Advance.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed, 32 FL OZ (1 QT) Not published in this source record 111 total cases. No lot or expiration date as bottles were not intended for distribution. Batch Numbers: BW3520316 (List Number 64248) and BW0970914 (List Number 66611).

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1021-2020
Event ID
85855
Status
Terminated
Classification
Class III
Company
Abbott Nutrition, Division of Abbott Laboratories
Product description
Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed, 32 FL OZ (1 QT)
Quantity
111 total cases.
Reason
Water filled bottles labeled as Similac Pro-Advance.
Recall initiation date
June 11, 2020
Report date
July 22, 2020
Classification date
Not published in this source record
Termination date
November 6, 2020
Distribution pattern
Products was distributed to the following states: CT, MD, NJ, NY, & PA.
UPC, lot, and code information
No lot or expiration date as bottles were not intended for distribution. Batch Numbers: BW3520316 (List Number 64248) and BW0970914 (List Number 66611).
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Abbott Nutrition, Division of Abbott Laboratories

Other recalls from Abbott Nutrition, Division of Abbott Laboratories

FDA Recall United States Terminated Historical recordClass II

Abbott Nutrition, Division of Abbott Laboratories

Product
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 p…
Published
September 18, 2019
Distribution
Distribution Centers in: Alabama, Iowa,…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Connecticut 1
Maryland 1
New Jersey 1
New York 1
Pennsylvania 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.