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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Sprigs Herbal Supplements Recalled for High Bacterial Growth

Agency Publication Date: October 6, 2022
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Summary

Eden's Answers Inc. is recalling 3,495 units of Sprigs brand herbal dietary supplements, including Dental Health, Honey Herbal Syrup, and Lil Ones Sleepy Time formulas. These products are being recalled because testing identified high levels of bacterial growth within the supplements. Consumers should return the products to the place of purchase for a refund or dispose of them immediately.

Risk

The supplements contain high levels of bacteria that could cause infections or gastrointestinal illness if consumed. This risk is particularly significant for children, the elderly, or individuals with compromised immune systems. No illnesses have been reported to date.

What You Should Do

  1. The recalled products are Sprigs brand herbal dietary supplements sold in glass amber bottles with black droppers, including Sprigs - Dental Health (8oz), Sprigs - Honey Herbal Syrup (8oz), and Sprigs - Lil Ones Sleepy Time (2oz).
  2. Identify if your product is affected by checking the packaging for the following identifiers: Dental Health Batch No. 1560-01-003 (Lot 1221107, Product No. 625031), Honey Herbal Syrup Batch No. 1470-01-003 (Lot 0222407, Product No. 625097), or Lil Ones Sleepy Time Batch No. 1615-01-002 (Lot 0322201, Product No. 8402).
  3. Return the product to the place of purchase for a full refund, throw it away, or contact Eden's Answers Inc. for further instructions.
  4. If you have already consumed these products and have health concerns, contact your healthcare provider or pharmacist.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Sprigs - Dental Health: Herbal Dietary Supplement (8oz)by Sprigs
Variants: 8oz glass amber bottles
Item Code:
625031
Lot Numbers:
1221107
Batch No. 1560-01-003

12 units per case; Recall #: F-0030-2023

Product: Sprigs - Honey Herbal Syrup: Herbal Dietary Supplement (8oz)by Sprigs
Variants: 8oz glass amber bottles
Item Code:
625097
Lot Numbers:
0222407
Batch No. 1470-01-003

12 units per case; Recall #: F-0031-2023

Product: Sprigs - Lil Ones Sleepy Time: Herbal Dietary Supplement (2oz)by Sprigs
Variants: 2oz glass amber bottles
Item Code:
8402
Lot Numbers:
0322201
Batch No. 1615-01-002

12 units per case; Recall #: F-0032-2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90902
Status: Resolved
Manufacturer: Eden's Answers Inc
Sold By: Retailers
Manufactured In: United States
Units Affected: 3 products (2594 units; 73 units; 828 units)
Distributed To: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, New Hampshire, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.