Nutraceutical International Corporation recalls KAL Amino Acid Complex with casein (milk protein) not clearly listed on ingredient labels. Products with use by dates before January 2019 are affected. Consumers should check labels and contact company for details.
Undeclared allergen, casein is a disclosed ingredient, but the word milk not specifically noted on the ingredient list
Nutraceutical International Corporation is recalling KAL Brand Amino Acid Complex products with use by dates before January 2019 because casein (milk protein) is not clearly listed on the ingredient labels. This poses a risk for people with milk allergies who may consume the product without knowing it contains milk.
Casein is a milk protein that can cause allergic reactions in sensitive individuals. The product does not clearly list 'milk' on the ingredient label, so people with milk allergies might unknowingly consume it.
People who have milk allergies or are sensitive to casein (milk protein) are at risk. Consumers who purchased KAL Amino Acid Complex with use by dates before January 2019 should check their labels.
Check for the UPC 021245516101 or Product #51610 on the label. Products with use by dates prior to January 2019 are affected.
Look for the UPC 021245516101 or Product #51610 on the label and verify the use by date.
No, the product contains casein (milk protein) but it is not clearly listed on the ingredient label, so people with milk allergies may unknowingly consume it.
Check the product label for the UPC 021245516101 or Product #51610 and use by date before January 2019. Contact Nutraceutical International Corporation for further instructions.
Products with use by dates prior to January 2019 and the UPC 021245516101 or Product #51610 are affected.
We’ve drafted a message you can send KAL to request your refund or repair — edit it as you like.
Subject: Recall F-3257-2015 — KAL KAL Hello, I own a KAL that is covered by recall F-3257-2015 from KAL. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
