MKS Enterprise LLC Recall: Undeclared Tadalafil
United States
TerminatedClass I
- Company
- MKS Enterprise LLC
- Product
- Dose Vital VIP Products Vital Honey With Caviar and Tongkat…
- Recall date
- July 18, 2022
- Terminated
- June 15, 2023
- Source
- FDA
Reason for recall
Undeclared Tadalafil
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder; 12 sachets-15g | Not published in this source record | 7 units | All lots |
Distribution
- Distributed to consumers in IL
- ND
- IN
- NC
- CA
- MD
- and VA.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1515-2022
- Event ID
- 90624
- Status
- Terminated
- Classification
- Class I
- Company
- MKS Enterprise LLC
- Product description
- Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder; 12 sachets-15g
- Quantity
- 7 units
- Reason
- Undeclared Tadalafil
- Recall initiation date
- July 18, 2022
- Report date
- August 10, 2022
- Classification date
- Not published in this source record
- Termination date
- June 15, 2023
- Distribution pattern
- Distributed to consumers in IL, ND, IN, NC, CA, MD, and VA.
- UPC, lot, and code information
- All lots
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: MKS Enterprise LLC
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Illinois | 1 |
| North Dakota | 1 |
| Indiana | 1 |
| North Carolina | 1 |
| California | 1 |
| Maryland | 1 |
| Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
