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Class II: temporary or reversible health riskTerminated

Abbott Nutrition, Division of Abbott Laboratories Similac Pro-Sensitive Recall

Similac Pro-Sensitive, 2 fl

Abbott Nutrition, Division of Abbott Laboratories · Columbus, OH

Risk level
Class II
Reported by FDA
Sep 18, 2019
Recall ID
F-2153-2019
Check your lot numberHow we source this data

Summary

Abbott Nutrition, Division of Abbott Laboratories recalled Similac Pro-Sensitive starting Aug 16, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2153-2019 on Sep 18, 2019. 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. Status: Terminated.

Why it was 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.

Product description

Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.

Lot numbers, UPCs & expiration codes

Carton Batch # 06108XK00; Bottle Batch # 02567X800

Where it was sold

Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2153-2019
Classification
Class II
Status
Terminated
Recall initiated
Aug 16, 2019
FDA report date
Sep 18, 2019
Quantity
13440 cartons but only 550 cartons (6600 bottles) affected
Recall type
Voluntary: Firm initiated
Recalling firm
Abbott Nutrition, Division of Abbott Laboratories

Original FDA data

Every field from FDA enforcement report F-2153-2019, exactly as published.

Show all FDA fields
City
Columbus
State
OH
Status
Terminated
Country
United States
Event ID
83608
Address
585 Cleveland Ave
Code information
Carton Batch # 06108XK00; Bottle Batch # 02567X800
Postal code
43215-1755
Report date
Sep 18, 2019
Product type
Food
Recall number
F-2153-2019
Classification
Class II
Recalling firm
Abbott Nutrition, Division of Abbott Laboratories
Product quantity
13440 cartons but only 550 cartons (6600 bottles) affected
Termination date
Dec 4, 2019
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Distribution pattern
Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin
Recall initiation date
Aug 16, 2019
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Sep 11, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2153-2019, published Sep 18, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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