Abbott Nutrition, Division of Abbott Laboratories recalls Similac Pro-Sensitive: label issue
Find the official FDA enforcement report
Recall at a glance
- Recalling company
- Abbott Nutrition, Division of Abbott Laboratories
- Location
- Columbus, OH
- Reported by FDA
- September 18, 2019
- Recall started
- August 16, 2019
- Risk class
- Class II
- Status (latest data we have)
- Terminated
- Type
- Voluntary: Firm initiated
- Category
- Other foods
- Reason type
- Labeling and quality
Is my product affected?
Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.
- Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Quantity: 13440 cartons but only 550 cartons (6600 bottles) affected
Codes: Carton Batch # 06108XK00; Bottle Batch # 02567X800
Where it was distributed
Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin
What to do
If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.
Frequently asked questions
What was recalled?
Abbott Nutrition, Division of Abbott Laboratories recalled 1 product, including Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton..
Why was it 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.
What does Class II mean?
FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Where was it sold or shipped?
Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin
What should I do if I have this product?
Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.
More recalls from Abbott Nutrition, Division of Abbott Laboratories
- Abbott Nutrition, Division of Abbott Laboratories recalls Similac Pro-Advance Infant Formula with Iron: label issue
July 22, 2020 · Abbott Nutrition, Division of Abbott Laboratories · Supplements and infant formula Class IIIWater filled bottles labeled as Similac Pro-Advance. Product: Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed, 32 FL OZ (1 QT)
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Sources
Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.