Carlise Lab
FDA import alert and refusal historySaint Michael, BarbadosFEI 3012522231
Recorded by FDA as CARLISE LAB
As of October 26, 2026, Carlise Lab is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 6, 2018, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Carlise Lab
1 record, newest first. Each line links to the FDA page it came from.
2018
- Import refusalRefused, Vitamin, n.e.c.UNAPPROVEDEntry 799-6264884-3Source
Refusal charges, in plain English
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Carlise Lab
- Is Carlise Lab on an FDA import alert?
- No listing for Carlise Lab appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Barbados page.
- Has FDA refused shipments from Carlise Lab?
- Yes. FDA refused 1 shipment line from Carlise Lab on June 6, 2018. The most recent, on June 6, 2018, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Carlise Lab's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Carlise Lab's FEI number?
- Carlise Lab's FDA Establishment Identifier (FEI) is 3012522231.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.