Bioreversa
FDA import alert and refusal historyTrois-Rivieres, CanadaFEI 3038620209
Recorded by FDA as BIOREVERSA
As of October 25, 2026, Bioreversa is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on July 29, 2025, most often for major food allergen not declared (ALLERGEN).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Bioreversa
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNSAFE COLLIST INGRECOLOR LBLGLACKS FIRMEntry SCS-1874659-9Show 2 linesHide lines
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNSAFE COLLIST INGRECOLOR LBLGLACKS FIRMALLERGENEntry SCS-1874659-9Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRELACKS FIRMALLERGENEntry SCS-1874659-9Source
Refusal charges, in plain English
- ALLERGEN2 refused lines
Major food allergen not declared
The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.
- LACKS FIRM2 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE2 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Bioreversa
- Is Bioreversa on an FDA import alert?
- No listing for Bioreversa appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Canada page.
- Has FDA refused shipments from Bioreversa?
- Yes. FDA refused 2 shipment lines from Bioreversa on July 29, 2025. The most recent, on July 29, 2025, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Bioreversa's shipments?
- The most frequent charges are ALLERGEN (major food allergen not declared, 2 lines) and LACKS FIRM (manufacturer name and address missing, 2 lines).
- What is Bioreversa's FEI number?
- Bioreversa's FDA Establishment Identifier (FEI) is 3038620209.
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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.