Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported September 18, 2019
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
Abbott Nutrition, Division of Abbott Laboratories recalled Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton. - a moderate-severity action.
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton. was recalled by Abbott Nutrition, Division of Abbott Laboratories in September 18, 2019. Reason: a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in…. Check the official notice for the remedy. Verify recall #F-2153-2019 with the FDA Food before acting.
The recall
Abbott Nutrition, Division of Abbott Laboratories issued this moderate-severity FDA Food recall-a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in….
- Moderate
- severity level
- Class II
- classification
- September 18, 2019
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2153-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2153-2019) was formally reported on September 18, 2019, with the manufacturer initiating the action on August 16, 2019. It is classified under Moderate severity (Class II), with a current status of Terminated. Abbott Nutrition, Division of Abbott Laboratories is listed as the recalling firm, operating out of Columbus, OH. Federal records list the affected scope as 13440 cartons but only 550 cartons (6600 bottles) affected.
The documented reason for this recall is: a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons. Distribution data in the federal record shows the product reached: Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
13440 cartons but only 550 cartons (6600 bottles) affected
Related Recalls
6
2 from same agency
Product description
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Reason for recall
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 Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2153-2019 |
| Date reported | September 18, 2019 |
| Date initiated | August 16, 2019 |
| Recalling firm | Abbott Nutrition, Division of Abbott Laboratories |
| Firm location | Columbus, OH |
| Affected scope | 13440 cartons but only 550 cartons (6600 bottles) affected |
| Distribution | Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-2153-2019) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.. Recalled by Abbott Nutrition, Division of Abbott Laboratories. Units affected: 13440 cartons but only 550 cartons (6600 bottles) affected.
Why was this product recalled? ▼
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 18, 2019. Severity: Moderate. Recall number: F-2153-2019.
Where was the recalled product distributed? ▼
Distribution: Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2153-2019) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 18, 2019. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.