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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

Absorb Health LLC: The firm was notified by the FDA that they failed to included a shellfish allergen on their ingredient panel.

Agency Publication Date: May 26, 2020
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Summary

Absorb Health LLC is recalling 70 bottles of its Advanced Joint Relief dietary supplement (510mg, 90 capsules) because the label fails to list a shellfish allergen. These products were sold in 17 states including AZ, CA, FL, GA, IA, MI, MN, NC, NM, NV, NY, OH, PA, TN, TX, VA, and WA. Consumers with shellfish allergies should check their supplement bottles for UPC 79056992863 immediately.

Risk

The product contains shellfish, a major food allergen, which is not declared on the ingredient panel. People who have an allergy or severe sensitivity to shellfish run the risk of a serious or life-threatening allergic reaction if they consume these capsules.

What You Should Do

  1. Check your supplement cabinet for 'Absorb Health Advanced Joint Relief Joint Health' in 510mg, 90-capsule bottles.
  2. Verify the UPC code on the bottle matches 79056992863 to determine if your product is affected.
  3. If you have a shellfish allergy or sensitivity, do not consume this product.
  4. Contact Absorb Health LLC or the retailer where the product was purchased for instructions on how to handle the affected supplement, as no specific remedy was provided in the official notice.
  5. For additional questions or to report a reaction, contact the FDA Consumer Complaint line at 1-888-723-3332 (1-888-SAFEFDA).

Affected Products

Product: Absorb Health Advanced Joint Relief Joint Health (510mg; 90 CAPSULES)
UPC Codes:
79056992863
Lot Numbers:
There are no codes for this product

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85242
Status: Active
Manufacturer: Absorb Health LLC
Manufactured In: United States
Units Affected: 70 bottles

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.

Find an Attorney

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 · 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.