FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on website.
Health risk
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
Action required
Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.
Recall closed · classified by the FDADistribution not listedMore supplements
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Hard Eight Nutrition LLCHenderson, NV, United States
UPC / barcodes
No UPC listed in the FDA enforcement record.
Lot / date codes
Lot: 121D1214, Exp: 12/13/18
Lot: 121E0629, Exp: 06/28/19.
Distribution area
Worldwide sales from website and Amazon. Foreign distribution to: " Australia " Austria " Canada " Czech Republic " Denmark " Finland " France " Germany " Iceland " Isle of Man " Italy " Japan " Liechtenstein " Luxembourg " Netherlands " New Zealand " Norway " South Africa " Sweden " Switzerland " The Philippines " United Kingdom
Canada, United Kingdom, Japan, Australia, Germany, France
Quantity affected
2, 100 units
Recall initiation
FDA report date: August 22, 2018
FDA recall number
F-1827-2018
Beyond the headline
The recall, in context
Hard Eight Nutrition LLC initiated this supplements recall on August 6, 2018. The FDA enforcement report states: FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on website. The FDA report lists distribution as: Worldwide sales from website and Amazon. Foreign distribution to: " Australia " Austria " Canada " Czech Republic " Denmark " Finland " France " Germany " Iceland " Isle of Man " Italy " Japan " Liechtenstein " Luxembourg " Netherlands " New Zealand " Norway " South Africa " Sweden " Switzerland " The Philippines " United Kingdom.
The FDA enforcement report describes the reason as: FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on website.
Bulksupplements.com Glucosamine Sulfate Potassium was made or distributed by Hard Eight Nutrition LLC in Henderson, NV, United States. This page reflects FDA report F-1827-2018, dated August 22, 2018.
Why this is a Class II recall
Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
FDA definition
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.
What to do now
1
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the lot and date codes against the table above.
3
Return or discard
Contact the retailer or recalling firm about a refund, and dispose of the product safely.
Consumer safety guide
Product safety recall
Symptoms to watch for
The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.
Higher-risk groups
Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.
What to do now
1Stop using or eating the product and keep it away from children and pets.
2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
3Seek medical advice if anyone develops severe or worrying symptoms after exposure.
Read the official source record for the specific hazard and instructions.
This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.
Frequently asked
Questions about this recall
7 answers
What is the Bulksupplements.com Glucosamine Sulfate Potassium recall?
Hard Eight Nutrition LLC recalled Bulksupplements.com Glucosamine Sulfate Potassium in an FDA Class II enforcement action reported as F-1827-2018. FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on website.
What are the symptoms of Product safety recall exposure?
The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.
Who is most at risk from Product safety recall?
Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.
What should I do if I bought this product?
Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.
How do I get a refund from Hard Eight Nutrition LLC?
Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1827-2018 and keep the packaging, lot code and proof of purchase if you have them.
Is the Hard Eight Nutrition LLC recall still active?
The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.
Where can I verify this recall?
This page is normalized from the openFDA enforcement record F-1827-2018. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.
Verify before you act.
VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.