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Class II: temporary or reversible health riskTerminated

Abbott Nutrition Similac Human Milk Fortifier Powder Recall

Similac Human Milk Fortifier Powder,

Abbott Nutrition · Columbus, OH

Risk level
Class II
Reported by FDA
Feb 26, 2014
Recall ID
F-1540-2014
Check your lot numberHow we source this data

Summary

Abbott Nutrition recalled Similac Human Milk Fortifier Powder starting Oct 11, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1540-2014 on Feb 26, 2014. Reason: Abbott Nutrition (AN) recalled this product from the Canadian market because some of the packets may have an incomplete seal which could allow air to enter the packet causing food oxidation and/or the powder to leak. Status: Terminated.

Why it was recalled

Abbott Nutrition (AN) recalled this product from the Canadian market because some of the packets may have an incomplete seal which could allow air to enter the packet causing food oxidation and/or the powder to leak

Product description

Similac Human Milk Fortifier Powder, .9 g packets. Label reads in part, "ADDITIONAL IRON MAY BE NECESSARY ADD ONLY TO HUMAN MILK - DO NOT ADD WATER NET WT 0.031 OZ (0.90g)***CONTAINS MILK AND SOY INGREDIENTS***USE BY***ABBOTT LABORATORIES"

Lot numbers, UPCs & expiration codes

Lot # L31056Z200, List # 54598-934(13) & USE BY 2015FE1; Lot L27385Z200 List # 54598-934(13) USE BY 2014OC1 & Lot L30698Z200 List # 54598 -934(13) USE BY 2015JA1

Where it was sold

All product in these lots were shipped to Canada.

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-1540-2014
Classification
Class II
Status
Terminated
Recall initiated
Oct 11, 2013
FDA report date
Feb 26, 2014
Quantity
Lot # L31056Z200-249cs/3 ctns/50/0.9 oz packets; Lot L27385Z200-328 cs/3 ctns/50/0.9 oz packets & Lot L30698Z200-349 cs/3 ctns/50/0.9 oz packets.
Recall type
Voluntary: Firm initiated
Recalling firm
Abbott Nutrition

Original FDA data

Every field from FDA enforcement report F-1540-2014, exactly as published.

Show all FDA fields
City
Columbus
State
OH
Status
Terminated
Country
United States
Event ID
67233
Address
3300 Stelzer Rd
Code information
Lot # L31056Z200, List # 54598-934(13) & USE BY 2015FE1; Lot L27385Z200 List # 54598-934(13) USE BY 2014OC1 & Lot L30698Z200 List # 54598 -934(13) USE BY 2015JA1
Postal code
43219-3034
Report date
Feb 26, 2014
Product type
Food
Recall number
F-1540-2014
Classification
Class II
Recalling firm
Abbott Nutrition
Product quantity
Lot # L31056Z200-249cs/3 ctns/50/0.9 oz packets; Lot L27385Z200-328 cs/3 ctns/50/0.9 oz packets & Lot L30698Z200-349 cs/3 ctns/50/0.9 oz packets.
Termination date
Apr 11, 2014
Reason for recall
Abbott Nutrition (AN) recalled this product from the Canadian market because some of the packets may have an incomplete seal which could allow air to enter the packet causing food oxidation and/or the powder to leak
Voluntary / mandated
Voluntary: Firm initiated
Product description
Similac Human Milk Fortifier Powder, .9 g packets. Label reads in part, "ADDITIONAL IRON MAY BE NECESSARY ADD ONLY TO HUMAN MILK - DO NOT ADD WATER NET WT 0.031 OZ (0.90g)***CONTAINS MILK AND SOY INGREDIENTS***USE BY***ABBOTT LABORATORIES"
Distribution pattern
All product in these lots were shipped to Canada.
Recall initiation date
Oct 11, 2013
Initial firm notification
Letter
Center classification date
Feb 20, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1540-2014, published Feb 26, 2014. View the source record (openFDA) · FDA enforcement reports

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

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