Caverflo Texas Trading
FDA import alert and refusal historySungai Petani, MalaysiaFEI 3011624043
Recorded by FDA as CAVERFLO TEXAS TRADING
As of October 26, 2026, Caverflo Texas Trading (Sungai Petani, Malaysia) is on the red list of FDA Import Alert 99-22 (Undeclared or mislabeled major food allergens) for caver flo natural herbal coffee, published by FDA on November 29, 2017, is also listed on Import Alert 99-39 (red list) and Import Alert 54-16 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Caverflo Texas Trading
3 records, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 99-22red listCaver Flo Natural Herbal CoffeeSource
- Import alert listingListed on Import Alert 99-39red listCaver Flo Natural Herbal CoffeeSource
- Import alert listingListed on Import Alert 54-16red listCaverFlo Natural Herbal CoffeeSource
Questions about Caverflo Texas Trading
- Is Caverflo Texas Trading on an FDA import alert?
- Yes. As of October 26, 2026, Caverflo Texas Trading is on the red list of FDA Import Alert 99-22, “Undeclared or mislabeled major food allergens”, for caver flo natural herbal coffee; FDA published the listing on November 29, 2017.
- Has FDA refused shipments from Caverflo Texas Trading?
- No FDA import refusals for Caverflo Texas Trading appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Caverflo Texas Trading's FEI number?
- Caverflo Texas Trading's FDA Establishment Identifier (FEI) is 3011624043.
- Can shipments from Caverflo Texas Trading still enter the U.S.?
- Shipments of caver flo natural herbal coffee from Caverflo Texas Trading can be detained without physical examination under Import Alert 99-22; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.