Fresh Recalls

FDAClass I · Food · Recall H-1196-2026 · Recalled August 12, 2026

Ashfiat Alharamain Energy Support 250ml/8fl recall — AKKARCO LLC

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Ashfiat Alharamain Energy Support 250ml/8fl
Company / brand
AKKARCO
Lot / serial / date codes
Batch No: ENGOT24 EXP: OCT 2028 UPC: 1234561870003
Distribution
The product was distributed nationwide through third-party e-commerce marketplace: Amazon.com
Agency product description and boundaries

Ashfiat Alharamain Energy Support 250ml/8fl. oz.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Undeclared tadalafil

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Ashfiat Alharamain Energy Support 250ml/8fl

3. Open the official notice or contact

Official recall ID
H-1196-2026
Brand
AKKARCO
Classification
Class I
Units affected
1052 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Lorton, VA, United States
Firm address
7361 Lockport Pl Ste D, 22079-1595

Identifying details (verbatim from the notice)

Product codes / lots
Batch No: ENGOT24 EXP: OCT 2028 UPC: 1234561870003
Distribution
The product was distributed nationwide through third-party e-commerce marketplace: Amazon.com
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
98392
Recall initiated
January 28, 2026
FDA classified
August 4, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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