🔍 RecallPedia

WANABANA APPLE CINNAMON FRUIT PUREE, Net Weight: 2.50 oz (71g) Pouches, 15 poches per carton, 3-pack carton in one box.

Class I - Dangerous
🍎 Food Recalled: October 29, 2023 WANABANA USA Produce

What Should You Do?

  1. Check if you have this product:
    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
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
WANABANA USA LLC
Reason for Recall:
North Carolina Department of Health and Human Services (NCDHHS) sampled product and found it to contain high levels of lead.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

WANABANA APPLE CINNAMON FRUIT PUREE, Net Weight: 2.50 oz (71g) Pouches, 15 poches per carton, 3-pack carton in one box.

Product Codes/Lot Numbers:

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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0402-2024

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