Dark Chocolate Almond Bark, 12/8oz.
Class I - DangerousWhat Should You Do?
- Check if you have this product: ALL NATURAL, NATURAL ALMONDS DARK CHOCOLATE , Product Number: 523089, Pack/Size: 12/7 oz., Best By Date: February 2017 October 2018, UPC: 94776139002 JLM TUB, TUB LG DARK CHOC BARK W/ALMOND, Product Number: 538814, Pack/Size:12/8 oz., Best By Date: February 2017 October 2018, UPC: 94776141722 WEIS, TUB WEIS LG DRK CHOCOLATE BARK W/ALMOND, Product Number: 866182, Pack/Size: 12/8 oz., Best By Date:February 2017 October 2018, UPC: 41497133253
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- JLM Manufacturing LLC
- Reason for Recall:
- JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Dark Chocolate Almond Bark, 12/8oz.
Product Codes/Lot Numbers:
ALL NATURAL, NATURAL ALMONDS DARK CHOCOLATE , Product Number: 523089, Pack/Size: 12/7 oz., Best By Date: February 2017 October 2018, UPC: 94776139002 JLM TUB, TUB LG DARK CHOC BARK W/ALMOND, Product Number: 538814, Pack/Size:12/8 oz., Best By Date: February 2017 October 2018, UPC: 94776141722 WEIS, TUB WEIS LG DRK CHOCOLATE BARK W/ALMOND, Product Number: 866182, Pack/Size: 12/8 oz., Best By Date:February 2017 October 2018, UPC: 41497133253
Distribution:
Distributed in: MI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0496-2018
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