Slayer Forever, LLC dba BUBS Naturals Recall: Firm was notified by supplier of Medium Chain Triglycerides (MCT) that it contained undeclared milk allergens. - F-0847-2021

🇺🇸 United States

1. May 7, 2021 - Recall initiated
2. August 18, 2021 - Reported by source
3. August 10, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0847-2021

Event ID

87914

Status

Terminated

Classification

Class I

Company

Slayer Forever, LLC dba BUBS Naturals

Product description

BUBS Naturals MCT OIL Powder, Medium Chain Triglycerides from 100% virgin Coconut Oil. Dietary Supplement 10.6 oz. Gusset Bags

Quantity

28,919 units

Reason

Firm was notified by supplier of Medium Chain Triglycerides (MCT) that it contained undeclared milk allergens.

Recall initiation date

May 7, 2021

Report date

August 18, 2021

Classification date

Not published in this source record

Termination date

August 10, 2021

Distribution pattern

Nationwide distribution through 2 distributors, Amazon and firm's online store.

UPC, lot, and code information

MCT50200004; Exp.1/22; MCT50200005 Exp. 1/22; MCT50200006 Exp. 1/22; MCT50200007 Exp. 1/22; MCT50200008 Exp. 1/22; MCT50200009 Exp. 1/22; MCT50200010 Exp. 1/22; MCT50200011 Exp. 5/22; MCT50200012 Exp. 5/22; MCT50200013 Exp. 5/22

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

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: Slayer Forever, LLC dba BUBS Naturals

Other recalls from Slayer Forever, LLC dba BUBS Naturals

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 I mean?

FDA classifies this recall as Class I. 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 August 10, 2021.

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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