Hard Eight Nutrition LLC Recall: Finished product possibly contaminated with pathogenic Staphylococcus aureus.

🇺🇸 United States

1. June 25, 2025 - Recall initiated
2. September 24, 2025 - Reported by source
3. November 5, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0619-2025

Event ID

97201

Status

Terminated

Classification

Class II

Company

Hard Eight Nutrition LLC

Product description

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.

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

Finished product possibly contaminated with pathogenic Staphylococcus aureus.

Recall initiation date

June 25, 2025

Report date

September 24, 2025

Classification date

Not published in this source record

Termination date

November 5, 2025

Distribution pattern

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

UPC, lot, and code information

UPC 849720004147; Lot Code/Batch Code: 2507803 Best Before Date: March 31, 2027

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Hard Eight Nutrition LLC

Other recalls from Hard Eight Nutrition LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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