Food FDA Class II Terminated Pathogen contamination
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
HARD EIGHT NUTRITION LLC Published Sep 24, 2025
Risk level
Class IIMay cause a temporary or reversible health problem; slight chance of serious harm.
Severity score 65/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- Do not eat, serve, or sell the affected product.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact HARD EIGHT NUTRITION LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall
Finished product possibly contaminated with pathogenic Staphylococcus aureus.
Hazards
Staphylococcus aureus · primary
Affected products (1)
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.
1001 units total=280/ 250g (8.8 oz) packages; 534 units of 500g (1.1 lbs); and 187 units of 1kg (2.2 lbs).
Lot codes: Code
Code info: Lot Code/Batch Code: 2507803 Best Before Date: March 31, 2027
Affected areas
Puerto Rico
Timeline
- InitiatedJun 25, 2025
- PublishedSep 24, 2025
- TerminatedNov 5, 2025
- Recall number
- H-0619-2025
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.