Class IITerminatedVoluntary: Firm initiated
HARD EIGHT NUTRITION LLC: food recall H-0619-2025
HARD EIGHT NUTRITION LLC of Henderson, NV recalled Brand name: BulkSupplements.com Generic name: Inositol. Dosage: 1 gram. Form: Powder. Route of administration: Oral.… Reason: Finished product possibly contaminated with pathogenic Staphylococcus aureus. The FDA listed it as Class II in its Enforcement Report dated Sep 24, 2025; distribution: Puerto Rico.
Record status as published: Terminated (terminated Nov 5, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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.
- Product quantity
- 1001 units total=280/ 250g (8.8 oz) packages; 534 units of 500g (1.1 lbs); and 187 units of 1kg (2.2 lbs).
- Reason for recall
- Finished product possibly contaminated with pathogenic Staphylococcus aureus.
- Codes, lots and dates on the package
- Lot Code/Batch Code: 2507803 Best Before Date: March 31, 2027
- Distribution pattern
- Distributed in the US including Puerto Rico and in Australia, Canada, Indonesia, Mexico, Netherlands, New Zealand, Norway, and United Kingdom.
- Recalling firm
- HARD EIGHT NUTRITION LLC, Henderson, NV
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jun 25, 2025 |
| Classified by the FDA | Sep 18, 2025 |
| Published in the Enforcement Report | Sep 24, 2025 |
| Terminated | Nov 5, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0619-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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