English Bay Blending
FDA import alert and refusal historyDelta, CanadaFEI 3003761761
As of October 26, 2026, English Bay Blending (Delta, Canada) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for gem sleep essentials chocolate cherry bites; gem daily essentials citrus ginger bites, published by FDA on February 29, 2024, and has 4 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-45 · red list
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for English Bay Blending
5 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalSource
Refused, 3 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.; Foods with supplemental nutrients added, with or without artifical sweetners and 1 moreLIST INGREDIRSEXMPTUNAPPROVEDUNSAFE ADDEntry 300-4871427-5Show 3 linesHide lines
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGREDIRSEXMPTUNAPPROVEDEntry 300-4871427-5Source
- Refused, Foods with supplemental nutrients added, with or without artifical sweetnersUNSAFE ADDEntry 300-4871427-5Source
- Refused, Chocolate candy bar, with nuts and fruitUNSAFE ADDEntry 300-4871427-5Source
- Import alert listingListed on Import Alert 99-45red listGEM Sleep Essentials Chocolate Cherry Bites; GEM Daily Essentials Citrus Ginger BitesSource
2020
Refusal charges, in plain English
- UNSAFE ADD2 refused lines
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.
- DIRSEXMPT1 refused line
DIRSEXMPT
- 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).
- PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that 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 English Bay Blending
- Is English Bay Blending on an FDA import alert?
- Yes. As of October 26, 2026, English Bay Blending is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for gem sleep essentials chocolate cherry bites; gem daily essentials citrus ginger bites; FDA published the listing on February 29, 2024.
- Has FDA refused shipments from English Bay Blending?
- Yes. FDA refused 4 shipment lines from English Bay Blending between March 6, 2020 and June 4, 2024. The most recent, on June 4, 2024, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse English Bay Blending's shipments?
- The most frequent charges are UNSAFE ADD (food additive unsafe under section 409, 2 lines) and DIRSEXMPT (dirsexmpt, 1 line).
- What is English Bay Blending's FEI number?
- English Bay Blending's FDA Establishment Identifier (FEI) is 3003761761.
- Can shipments from English Bay Blending still enter the U.S.?
- Shipments of gem sleep essentials chocolate cherry bites; gem daily essentials citrus ginger bites from English Bay Blending can be detained without physical examination under Import Alert 99-45; 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.