Abbott Nutrition, Division of Abbott Laboratories Recall: Water filled bottles labeled as Similac Pro-Advance. - F-1021-2020
🇺🇸 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.
- Recall initiated
- Reported by source
- 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
A map highlighting the states named in the source's distribution description.
Distributed
No data published
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.
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?
FDA classifies this recall as Class III. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for
current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of November 6, 2020.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.
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