CT Health Solutions, LLC Recall: Due to different color of powder in capsules. Firm's evaluation determined product low potency.
United States
TerminatedClass III
- Company
- CT Health Solutions, LLC
- Product
- We Like Vitamins, Lycopene 50 mg, Dietary Supplement, 200 Ca…
- Recall date
- March 27, 2020
- Terminated
- August 27, 2020
- Source
- FDA
Reason for recall
Due to different color of powder in capsules. Firm's evaluation determined product low potency.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| We Like Vitamins, Lycopene 50 mg, Dietary Supplement, 200 Capsules | Not published in this source record | 1500 Bottles | Dec/2023, Lot# 02121902 |
Distribution
- Product was distributed to 1 consignee in Michigan (Domestic distribution only)
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0923-2020
- Event ID
- 85358
- Status
- Terminated
- Classification
- Class III
- Company
- CT Health Solutions, LLC
- Product description
- We Like Vitamins, Lycopene 50 mg, Dietary Supplement, 200 Capsules
- Quantity
- 1500 Bottles
- Reason
- Due to different color of powder in capsules. Firm's evaluation determined product low potency.
- Recall initiation date
- March 27, 2020
- Report date
- April 22, 2020
- Classification date
- Not published in this source record
- Termination date
- August 27, 2020
- Distribution pattern
- Product was distributed to 1 consignee in Michigan (Domestic distribution only)
- UPC, lot, and code information
- Dec/2023, Lot# 02121902
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: CT Health Solutions, LLC
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
