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

🇺🇸 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.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

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?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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.

• Email
• X / Twitter
• Facebook