CPSC
Skip Hop Recalls Baby Sesame Street Elmo Silicone Teethers Due to Risk of Serious Injury or Death from Choking Hazard
The black eyes can detach from the recalled teether if frozen, posing a risk of serious injury or death from a choking hazard.
FDAClass I
a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron;… Recalled: Product may be contaminated with Clostridium botulinum.
a.) nara organics brand was recalled on June 13, 2026 in cooperation with the U.S. Food and Drug Administration because product may be contaminated with Clostridium botulinum..
Is my unit affected?
a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 24.7 OZ (700 G); UPC: 860013251901 b.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 14.1 OZ (400 G); UPC: 860013251918
Model, lot & date codes to check
Recalled Lot Codes - 408125075E14F2 - 708125076E14F2 - 708125083E14F2 - 408125139E14F2 - 708125141E14F2 - 708125145E14F2 - 708125174E14F2 - 709125273E14F2 - 709125280E14F2 - 709125288E14F2 - 409125307E14F2 - 70926019ENNB - 70926029ENNB - 70926035ENNB - 70926039ENNB - 70926042ENNB Use-By dates span March 16, 2027 - February 11, 2028
Units affected: 377,610 cans
Where it was sold: nationwide
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
What's the hazard?
Product may be contaminated with Clostridium botulinum.
Class I is the most serious FDA recall level: using or being exposed to the product could cause serious health problems or death.
Your remedy & how to claim it
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: NARA ORGANICS INC
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Official recall notice
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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