Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Recalling firm: Abbott Nutrition, Division of Abbott Laboratories
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Dec 4, 2019.
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FDA code information
Carton Batch # 06108XK00; Bottle Batch # 02567X800
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Full FDA record and distribution details
Original product description
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| batch | 02567X800 | Carton Batch # 06108XK00; Bottle Batch # 02567X800 |
| batch | 06108XK00 | Carton Batch # 06108XK00; Bottle Batch # 02567X800 |
Original FDA recall reason
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
Recall details
- Recall number
- F-2153-2019
- Event ID
- 83608
- FDA status
- Terminated
- Initiated
- Aug 16, 2019
- Reported
- Sep 18, 2019
- Classified
- Sep 11, 2019
- Terminated
- Dec 4, 2019
- Quantity
- 13440 cartons but only 550 cartons (6600 bottles) affected
- Location
- Columbus, OH, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin
Data updated September 16, 2026. View official FDA data ↗
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