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Class I: serious health riskTerminated

Shopaax.com Kingdom Honey Royal Honey VIP The Ultimate Recall

Kingdom Honey Royal Honey VIP The Ultimate Power Source

Shopaax.com · Newark, DE

Risk level
Class I
Reported by FDA
Aug 10, 2022
Recall ID
F-1514-2022
Check your lot numberHow we source this data

Summary

Shopaax.com recalled Kingdom Honey Royal Honey VIP The Ultimate starting Jul 13, 2022. The FDA classified it as Class I (serious health risk) and published enforcement report F-1514-2022 on Aug 10, 2022. Reason: Undeclared Sildenafil. Status: Terminated.

Why it was recalled

Undeclared Sildenafil

Product description

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

Lot numbers, UPCs & expiration codes

All lots

Where it was sold

Distributed to customers nationwide

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1514-2022
Classification
Class I
Status
Terminated
Recall initiated
Jul 13, 2022
FDA report date
Aug 10, 2022
Quantity
unknown
Recall type
Voluntary: Firm initiated
Recalling firm
Shopaax.com

Original FDA data

Every field from FDA enforcement report F-1514-2022, exactly as published.

Show all FDA fields
City
Newark
State
DE
Status
Terminated
Country
United States
Event ID
90595
Address
2 Burleigh Ct
Address (line 2)
Apt A5
Code information
All lots
Postal code
19702-2658
Report date
Aug 10, 2022
Product type
Food
Recall number
F-1514-2022
Classification
Class I
Recalling firm
Shopaax.com
Product quantity
unknown
Termination date
Sep 12, 2024
Reason for recall
Undeclared Sildenafil
Voluntary / mandated
Voluntary: Firm initiated
Product description
Kingdom Honey Royal Honey VIP The Ultimate Power Source; 12 sachets-20g; UPC 555755 800036
Distribution pattern
Distributed to customers nationwide
Recall initiation date
Jul 13, 2022
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Aug 1, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1514-2022, published Aug 10, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

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