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
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
- Brand
- Ashfiat Alharamain
- 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 2026 | Recall initiated by company | |
| 4 Aug 2026 | Classified by FDA | +188 days |
| 12 Aug 2026 | Published 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
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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