similac baby formula recalled
The recalled products are. The company issued a recall of products made at its Sturgis Michigan facility.
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Similac Advance Step 1 Milk-Based Iron-Fortified Infant Formula Powder Similac Advance Step 2 Milk-Based Iron-Fortified and Calcium-Enriched Infant Formula Powder Similac Alimentum Step 1 Hypoallergenic Infant Formula Powder Similac Human Milk Fortifier Powder.
. Products being recalled throughout Canada include. FDA warns about recalled baby formula amid investigation of 4 illnesses Specifically the FDA is advising consumers to check containers of Similac Alimentum or EleCare powdered infant formulas. The first two digits of the code are 22 through 37 the code on the container contains K8 SH or Z2 the expiration date is 4-1-2022 APR 2022 or later.
The FDA is urging consumers not to purchase or use certain Similac Alimentum or EleCare powdered infant formulas produced at Abbott Nutritions Sturgis Michigan facility while. Heres how to tell if you have a recalled container of Similac Alimentum and EleCare. Similac Advance Step 1 Milk-Based Iron-Fortified Infant Formula Powder Similac Advance Step 2 Milk-Based Iron-Fortified and Calcium-Enriched Infant Formula Powder Similac Alimentum Step 1 Hypoallergenic Infant Formula Powder Similac Human Milk Fortifier Powder.
Similac Advance Step 1 Milk-Based Iron-Fortified Infant Formula Powder. AP Feb 17 Abbott Laboratories said on Thursday it was recalling powdered baby formulas including Similac made at a Michigan facility after four consumers complained about bacterial infections. Abbott Nutrition issued voluntary recalls of their popular Similac Alimentum and EleCare formulas after four infants were hospitalized with bacterial infections.
The recall announced Thursday is for select lots of Similac Alimentum and EleCare formulas that were manufactured at an Abbott facility in Sturgis Michigan. Reuters - Abbott Laboratories said on Thursday it was recalling powdered baby formulas including Similac made at a Michigan facility after four consumers complained about bacterial infections in. The Food and Drug Administration.
0 55325 00076. February 17 2022 346 PM 1 min read.
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