CLASS I Food recall · Reported 10 Aug 2022 · FDA Enforcement Report

Kingdom Honey Royal Honey VIP The Ultimate Power Source recalled

Shopaax.com is recalling Kingdom Honey Royal Honey VIP The Ultimate Power Source, distributed nationwide in the US. The recall was initiated on 13 Jul 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lots
Quantity recalledunknown

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
F-1514-2022
FDA event ID
90595
Recalling firm
Shopaax.com, Newark, DE
Brand
Kingdom
Classification
Class I
Status
Terminated
Recall initiated
13 Jul 2022
FDA classified
1 Aug 2022
Reported
10 Aug 2022
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
Honey & Syrup

Timeline

13 Jul 2022Recall initiated by company
1 Aug 2022Classified by FDA+19 days
10 Aug 2022Published in enforcement report+9 days

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

Reason for recall

Undeclared Sildenafil

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

Kingdom Honey Royal Honey VIP The Ultimate Power Source; 12 sachets-20g; UPC 555755 800036

Where it was distributed

Distributed to customers nationwide

Nationwide

Questions about this recall

Why was it recalled?

Undeclared Sildenafil

Which lots are affected?

All lots

Where was it sold?

Distributed to customers nationwide

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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