Ararat Imambayeldy; 18.3 oz. glass jar; Ingredient: Eggplant, tomato paste, onions, vegetable oil, garlic, green salt Product of Armenia; Exclusively imported and distributed by: Kradjian Importing Co., Inc. Glendale, CA
Class I - DangerousWhat Should You Do?
- Check if you have this product: Batch number- 84- 08/14/17 Best by August 2020; Batch number- 85- 08/15/17 Best by August 2020; Batch number- 86-08/16/17 Best by August 2020; Batch number- 87-08/18/17 Best by August 2020; Batch number- 88-08/21/17 Best by August 2020; Batch number- 89-08/22/17 Best by August 2020.
- 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:
- Artashes LLC
- Reason for Recall:
- FDA foreign inspection found pH levels in four products to be above their scheduled process.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Ararat Imambayeldy; 18.3 oz. glass jar; Ingredient: Eggplant, tomato paste, onions, vegetable oil, garlic, green salt Product of Armenia; Exclusively imported and distributed by: Kradjian Importing Co., Inc. Glendale, CA
Product Codes/Lot Numbers:
Batch number- 84- 08/14/17 Best by August 2020; Batch number- 85- 08/15/17 Best by August 2020; Batch number- 86-08/16/17 Best by August 2020; Batch number- 87-08/18/17 Best by August 2020; Batch number- 88-08/21/17 Best by August 2020; Batch number- 89-08/22/17 Best by August 2020.
Distribution:
Distributed in: CA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1902-2018
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