SupplierRadar

Zurich Pharma Inc

FDA import alert and refusal historyWindsor, CanadaFEI 3011799128

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Zurich Pharma Inc.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectZurich Pharma In added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Zurich Pharma Inc is not on any FDA import alert in SupplierRadar's records; FDA refused 8 of its shipment lines between January 26, 2018 and April 1, 2022, most often for no u.s. adverse event contact on supplement label (NCONTACT).

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. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Zurich Pharma Inc

8 records, newest first. Each line links to the FDA page it came from.

2022

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 300-2954350-1
    Source
  2. Import refusal
    Refused, Vitamin b12 (cyanocobalamin)LABELINGEntry 300-2925437-2
    Source

2018

  1. Import refusal
    Refused, Royal jelly (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.)NCONTACTUNAPPROVEDEntry UPS-7127375-0
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIETARYLBLNCONTACTLABELINGDIETARYINGEntry 300-1177388-4Show 2 lines
    Source
  3. Import refusal
    Refused, Royal jelly (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.)NCONTACTUNAPPROVEDEntry UPS-7219232-2
    Source
  4. Import refusal
    Refused, Royal jelly (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.)NCONTACTUNAPPROVEDEntry UPS-7138104-1
    Source
  5. Import refusal
    Refused, Royal jelly (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.)NCONTACTUNAPPROVEDEntry UPS-7127418-8
    Source

Refusal charges, in plain English

  • NCONTACT6 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • UNAPPROVED5 refused lines

    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.

  • LABELING3 refused lines

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • 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).

Questions about Zurich Pharma Inc

Is Zurich Pharma Inc on an FDA import alert?
No listing for Zurich Pharma Inc appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Canada page.
Has FDA refused shipments from Zurich Pharma Inc?
Yes. FDA refused 8 shipment lines from Zurich Pharma Inc between January 26, 2018 and April 1, 2022. The most recent, on April 1, 2022, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Zurich Pharma Inc's shipments?
The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 6 lines) and UNAPPROVED (unapproved new drug, 5 lines).
What is Zurich Pharma Inc's FEI number?
Zurich Pharma Inc's FDA Establishment Identifier (FEI) is 3011799128.

Buying from Zurich Pharma Inc?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Zurich Pharma Inc.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectZurich Pharma In added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.