Similac Pro-Sensitive 2 fl oz bottles recalled due to packaging mix-up
Abbott Nutrition recalls Similac Pro-Sensitive 2 fl oz plastic bottles packed 12 per carton from a specific batch due to packaging mix-up with Pro-Advance bottles.
Lower-risk 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.
Contact the company
What happened, in plain English
Abbott Nutrition is recalling Similac Pro-Sensitive 2 fl oz plastic bottles that were mistakenly packaged with Pro-Advance bottles. This mix-up means some bottles could be unsafe for use as they are not the correct product type. Read more at govinfonow.com/recall/16751-similac-pro-sensitive-2-fl-oz-bottles-recalled-due-to.
Source Summary by GovInfoNow · govinfonow.com/recall/16751-similac-pro-sensitive-2-fl-oz-bottles-recalled-due-to · Updated October 5, 2026 · FDA enforcement record: FDA #F-2153-2019
Cite this page
“Similac Pro-Sensitive 2 fl oz bottles recalled due to packaging mix-up.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16751-similac-pro-sensitive-2-fl-oz-bottles-recalled-due-to. Based on FDA recall #F-2153-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2153-2019%22&limit=1).
Why it’s dangerous
The recalled bottles were mistakenly packaged with Similac Pro-Advance bottles instead of the intended Similac Pro-Sensitive bottles. This mix-up could lead to infants receiving the incorrect formula type, which may not be suitable for their needs.
Who’s affected
Parents or caregivers of infants using Similac Pro-Sensitive formula. Infants who have received formula from the recalled bottles are at risk of receiving the wrong product type.
How to tell if you have this one
Check for carton batch number 06108XK00 and bottle batch number 02567X800 on the product packaging. The product is Similac Pro-Sensitive 2 fl oz plastic bottles packed 12 per carton.
- Brand
Abbott Nutrition- Category
Food
What to do — step by step
Check Product Details
Look for carton batch number 06108XK00 and bottle batch number 02567X800 on the product packaging.
Where it went and when
Where it was distributed
Distributed in 8 states.
FDA distribution: “Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Iowa, New York, North Carolina, Ohio, South Carolina, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Are these bottles safe to use?
The recall is due to a packaging mix-up with Pro-Advance bottles, not a safety hazard. The bottles themselves are safe but may contain the wrong formula type.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-2153-2019 (August 16, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2153-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.