🔍 RecallPedia

"Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net Wt. 16 oz (454 g) packaged in a green plastic bag; and 12oz (340g) packaged in a clear plastic box

Class I - Dangerous
Recalled: November 2, 2021 Murray International Trading Co. Other Foods

What Should You Do?

  1. Check if you have this product:
    16oz Green Plastic Bag Codes: 767533-91001; 767533-91005; 767533-91011; 767533-91018; 767533-91019; 767533-91020; 767533-91049; 767533-91050; 767533-91057; 767533-91060; 767533-91062; 767533-91068; 767533-91070; 767533-91071 12oz Clear Plastic Box Code: 767533-20097
  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:
Murray International Trading Co., Inc.
Reason for Recall:
Product contains elevated levels of lead and cadmium
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

"Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net Wt. 16 oz (454 g) packaged in a green plastic bag; and 12oz (340g) packaged in a clear plastic box

Product Codes/Lot Numbers:

16oz Green Plastic Bag Codes: 767533-91001; 767533-91005; 767533-91011; 767533-91018; 767533-91019; 767533-91020; 767533-91049; 767533-91050; 767533-91057; 767533-91060; 767533-91062; 767533-91068; 767533-91070; 767533-91071 12oz Clear Plastic Box Code: 767533-20097

Distribution:

Distributed in: NY, NJ, PA, MA, CT, DC, VA, DE, RI, FL, GA, MI, IL, OH, TX

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0275-2022

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