WANABANA APPLE CINNAMON FRUIT PUREE, Net Weight: 2.50 oz (71g) Pouches, 15 poches per carton, 3-pack carton in one box.
Summary
The FDA issued a Class I for WANABANA APPLE CINNAMON FRUIT PUREE, Net Weight: 2.50 oz (71g) Pouches, 15 poche by WANABANA USA LLC. Reason: North Carolina Department of Health and Human Services (NCDHHS) sampled product and found it to contain high levels of lead..
Details
Source
Food Recall
External ID
F-0402-2024
Action Date
2023-11-15
Status
Terminated
Category
food
Product Description
WANABANA APPLE CINNAMON FRUIT PUREE, Net Weight: 2.50 oz (71g) Pouches, 15 poches per carton, 3-pack carton in one box.
Lot/Code Info: Batch/Lot: 10022:31, 11022:08, 11022:09, 11022:10, 11022:12, 11022:14, 11022:15, 11022:16, 12022:23, 01023:03, 01023:17, 01023:23,01023:27,01023:30,01023:31, 02023:07,02023:18, 04023:23, 04023:24,04023:25,04023:26, 05023:08,05023:09,05023:10,05023:11,05023:15, 05023:29, 06023:02, 06023:03, 07023:21, 08023:06, 08023:10, 08023:25, 09023:27, 10023:19
Quantity Affected: 2,998,088 units (total)
Reason for Recall
North Carolina Department of Health and Human Services (NCDHHS) sampled product and found it to contain high levels of lead.
Distribution
Virginia, Kentucky, California, Puerto Rico, United Arab Emirates, Cuba
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-29
Company
Jacksonville, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
WANABANA USA LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (WANABANA USA LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does WANABANA USA LLC have FDA actions?
WANABANA USA LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0402-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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