Fungi Perfecti LLC Recall: Host Defense MycoBotanicals Blood Sugar, 60 ct. bottles, is recalled due to undeclared wheat. - F-1231-2019

🇺🇸 United States

1. February 28, 2019 - Recall initiated
2. April 10, 2019 - Reported by source
3. June 28, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1231-2019

Event ID

82297

Status

Terminated

Classification

Class II

Company

Fungi Perfecti LLC

Product description

Host Defense MycoBotanicals Blood Sugar, dietary supplement, 500mg capsules, 60 ct per bottle, serving size 2 capsules per day. UPC: 6 33422 70474 6 (distributed in US) UPC: 8 22078 71303 9 (distributed in Canada) The product is labeled in parts: "***HOST DEFENSE MYCO BOTANICALS BLOOD SUGAR ***Made with Organic Mushroom Mycelium, Gymnema & Cinnamon, 60 Vegetarian Capsules Dietary Supplement***GLUTEN FREE*** Distributed by Fungi Perfecti, LLC PO BOX 7634 Olympia, WA 98507***.

Quantity

11,042 bottles

Reason

Host Defense MycoBotanicals Blood Sugar, 60 ct. bottles, is recalled due to undeclared wheat.

Recall initiation date

February 28, 2019

Report date

April 10, 2019

Classification date

Not published in this source record

Termination date

June 28, 2019

Distribution pattern

Distributed in the US nationwide. Also distributed in Norway and Canada

UPC, lot, and code information

100217 EXP: 10/20 101718 EXP: 10/21 080918 EXP: 08/21 (Canada) Lot code is the date of encapsulation, expiration is set as month/year 3 years from month of manufacture .

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Fungi Perfecti LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of June 28, 2019.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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