Biocaro Pharmaceutical Co., Ltd
FDA import alert and refusal historyZhengzhou, ChinaFEI 3015409380
As of October 25, 2026, Biocaro Pharmaceutical Co., Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between June 27, 2019 and May 11, 2023, most often for manufacturer name and address missing (LACKS FIRM).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Soft candy with fruit, n.e.c. (without chocolate) · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Biocaro Pharmaceutical Co., Ltd
5 records, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, Soft candy with fruit, n.e.c. (without chocolate)LIST INGREDIETARYLBLSTD IDENTLACKS FIRMEntry EPS-2137379-8Source
2021
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LACKS FIRMNUTRIT LBLEntry 799-1134427-2Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LACKS FIRMNUTRIT LBLEntry 799-1087167-1Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGREINCONSPICULACKS FIRMDIETARYINGUNAPPROVEDEntry 799-1113016-8Source
2019
Refusal charges, in plain English
- LACKS FIRM4 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).
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- DIETARYING1 refused line
Dietary ingredients not listed
The dietary supplement label appeared not to list each dietary ingredient and its quantity, or the total quantity of a proprietary blend.
- DIETARYLBL1 refused line
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- INCONSPICU1 refused line
Required information not conspicuous
Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.
- MELAMINE1 refused line
Melamine
The product appeared to contain melamine or a melamine analog, which is an unsafe food additive within the meaning of section 409 of the FD&C Act.
- STD IDENT1 refused line
Does not conform to standard of identity
The product appeared to be represented as a food that has an FDA standard of identity, but not to conform to that standard.
Questions about Biocaro Pharmaceutical Co., Ltd
- Is Biocaro Pharmaceutical Co., Ltd on an FDA import alert?
- No listing for Biocaro Pharmaceutical Co., Ltd appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the China page.
- Has FDA refused shipments from Biocaro Pharmaceutical Co., Ltd?
- Yes. FDA refused 5 shipment lines from Biocaro Pharmaceutical Co., Ltd between June 27, 2019 and May 11, 2023. The most recent, on May 11, 2023, was soft candy with fruit, n.e.c. (without chocolate), charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Biocaro Pharmaceutical Co., Ltd's shipments?
- The most frequent charges are LACKS FIRM (manufacturer name and address missing, 4 lines) and LIST INGRE (ingredients not listed, 2 lines).
- What is Biocaro Pharmaceutical Co., Ltd's FEI number?
- Biocaro Pharmaceutical Co., Ltd's FDA Establishment Identifier (FEI) is 3015409380.
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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.