Dietary Supplements packaged in the following configurations: (1) Bulk 6916 Shanghai DigestiveBlend powder, packaged in varying quantities in poly bags within fiber drums (SKU 83274); (2) Bulk 6916 WEDAR DIGESTIVEBLEND powder, packaged in varying quantities in poly bags within fiber drums (SKU 82426);

Class I - Dangerous
Recalled: October 30, 2013 National Enzyme Supplements Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #'s: 83274014, 83274015, 83274016, 83274017, 83274018, 83274019, 83274020, 83274021, 83274022, 83274023, 83274025, 83274026, 83274027, 83274028, 83274035, 82426059, and 82426060
  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:
National Enzyme Co
Reason for Recall:
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Dietary Supplements packaged in the following configurations: (1) Bulk 6916 Shanghai DigestiveBlend powder, packaged in varying quantities in poly bags within fiber drums (SKU 83274); (2) Bulk 6916 WEDAR DIGESTIVEBLEND powder, packaged in varying quantities in poly bags within fiber drums (SKU 82426);

Product Codes/Lot Numbers:

Lot #'s: 83274014, 83274015, 83274016, 83274017, 83274018, 83274019, 83274020, 83274021, 83274022, 83274023, 83274025, 83274026, 83274027, 83274028, 83274035, 82426059, and 82426060

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0753-2014

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