CLASS I ONGOING Food recall · Reported 12 Aug 2026 · FDA Enforcement Report

Ashfiat Alharamain Energy Support recalled by Akkarco

Akkarco is recalling Ashfiat Alharamain Energy Support, distributed nationwide in the US. The recall was initiated on 28 Jan 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBatch No: ENGOT24 EXP: OCT 2028 UPC: 1234561870003
Quantity recalled1052 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-1196-2026
FDA event ID
98392
Recalling firm
Akkarco, Lorton, VA
Classification
Class I
Status
Ongoing
Recall initiated
28 Jan 2026
FDA classified
4 Aug 2026
Reported
12 Aug 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Allergens
Product category
Other

Timeline

28 Jan 2026Recall initiated by company
4 Aug 2026Classified by FDA+188 days
12 Aug 2026Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared tadalafil

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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

Where it was distributed

The product was distributed nationwide through third-party e-commerce marketplace: Amazon.com

Nationwide

Stores named: Amazon, Online Retailers

Questions about this recall

Why was it recalled?

Undeclared tadalafil

Which lots are affected?

Batch No: ENGOT24 EXP: OCT 2028 UPC: 1234561870003

Where was it sold?

The product was distributed nationwide through third-party e-commerce marketplace: Amazon.com

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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