Qpharm Inc.
FDA import alert and refusal historyCambridge, CanadaFEI 3002815077
As of October 26, 2026, Qpharm Inc. (Cambridge, Canada) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for health supplement rhoziva, published by FDA on August 11, 2017, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- Herbals & botanicals (not teas), n.e.c. · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Qpharm Inc.
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Herbals & botanicals (not teas), n.e.c.LIST INGREDIRSEXMPTDIETARYLBLLACKS FIRMLACKS N/CNCONTACTNUTRIT LBLUNAPPROVEDEntry UPS-3866631-0Source
- Import alert listingListed on Import Alert 99-39red listHealth Supplement RhozivaSource
Refusal charges, in plain English
- 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).
- DIRSEXMPT1 refused line
DIRSEXMPT
- LACKS FIRM1 refused line
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.
- LACKS N/C1 refused line
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- LIST INGRE1 refused line
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).
- NCONTACT1 refused line
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.
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- 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 Qpharm Inc.
- Is Qpharm Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Qpharm Inc. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for health supplement rhoziva; FDA published the listing on August 11, 2017.
- Has FDA refused shipments from Qpharm Inc.?
- Yes. FDA refused 1 shipment line from Qpharm Inc. on August 24, 2017. The most recent, on August 24, 2017, was herbals & botanicals (not teas), n.e.c., charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Qpharm Inc.'s shipments?
- The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 1 line) and DIRSEXMPT (dirsexmpt, 1 line).
- What is Qpharm Inc.'s FEI number?
- Qpharm Inc.'s FDA Establishment Identifier (FEI) is 3002815077.
- Can shipments from Qpharm Inc. still enter the U.S.?
- Shipments of health supplement rhoziva from Qpharm Inc. can be detained without physical examination under Import Alert 99-39; 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.