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FDA source record Class II Terminated

Brand name: BulkSupplements.com Generic name: Inositol. Dosage: 1 gram. Form: Powder. Route of administration: Oral. Packaging is flexible plastic. Net Wt.: 8.8 oz (250 grams)...

Recall Date: 2025-06-25 Recalling Firm: HARD EIGHT NUTRITION LLC Record Ref: H-0619-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Brand name: BulkSupplements.com Generic name: Inositol. Dosage: 1 gram. Form: Powder. Route of administration: Oral. Packaging is flexible plastic. Net Wt.: 8.8 oz (250 grams)... and names HARD EIGHT NUTRITION LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: HARD EIGHT NUTRITION LLC
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2025-06-25
Best identifiers to check for a FDA record

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Product Description & Identification

Brand name: BulkSupplements.com Generic name: Inositol. Dosage: 1 gram. Form: Powder. Route of administration: Oral. Packaging is flexible plastic. Net Wt.: 8.8 oz (250 grams), 1.1 lbs (500 grams), 2.2 lbs (1 kilogram). UPC: 849720004147, 849720004154, 849720004161 Firm Name/Address: Hard Eight Nutrition LLC dBa BulkSupplements.com 640 W Lake Mead Pkwy Henderson, NV 89015, USA.

Reason for Recall / Hazard Identified

Finished product possibly contaminated with pathogenic Staphylococcus aureus.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Distributed in the US including Puerto Rico and in Australia, Canada, Indonesia, Mexico, Netherlands, New Zealand, Norway, and United Kingdom.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
H-0619-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
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