TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g) UPC: 749735002186 Product is a powder packed metal cans. 6
Summary
The FDA issued a Class II for TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g) UPC: 749735002186 P by Nutricia North America. Reason: Infant formula contains undeclared tyrosine.
Details
Source
Food Recall
External ID
F-0989-2023
Action Date
2023-06-28
Status
Terminated
Category
food
Product Description
TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g) UPC: 749735002186 Product is a powder packed metal cans. 6 cans per case.
Lot/Code Info: Expiration date: 03/30/2024 Batch/lot code 101175408 Case EAN code: 749735102183 Vendor product code: 90218
Quantity Affected: 94 cans
Reason for Recall
Infant formula contains undeclared tyrosine
Distribution
Alaska, California, Connecticut, Florida, Illinois, Kansas, Louisiana, Maine, Minnesota, Mississippi, Nebraska, New Mexico, New York, Ohio, Pennsylvania, Tennessee, Texas, Utah, Virginia, Vermont, Washington and Puerto Rico.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-17
Company
Rockville, MD
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Nutricia North America has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Nutricia North America) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Nutricia North America have FDA actions?
Nutricia North America has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0989-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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