NATURE'S SUNSHINE PRODUCTS Recall: The firm was notified by its ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.

🇺🇸 United States

1. April 12, 2021 - Recall initiated
2. May 19, 2021 - Reported by source
3. April 5, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0791-2021

Event ID

87714

Status

Terminated

Classification

Class I

Company

NATURE'S SUNSHINE PRODUCTS

Product description

Love & Peas Protein Rich Meal Replacement, 1 LB 8 OZ (675 G) bag, Nature's Sunshine Products, Inc., Spanish Fork, Utah, 84660 (800) 223-8225, naturessunshine.com, UPC 0 99904 03082 4

Quantity

6,069 bags

Reason

The firm was notified by its ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.

Recall initiation date

April 12, 2021

Report date

May 19, 2021

Classification date

Not published in this source record

Termination date

April 5, 2022

Distribution pattern

Nationwide. Canada.

UPC, lot, and code information

Lot #: 001220292 Exp.: 29-DEC-2022 Lot #: 001222059 Exp.: 10-JAN-2023 Lot #: 001215380 Exp.: 09-NOV-2022 Lot #: 001218022 Exp.: 07-DEC-2022 Lot #: 001220084 Exp.: 23-DEC-2022 Lot #: 001224031 Exp.: 27-JAN-2023

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

Other products recalled under this same event

This recall shares FDA event ID 87714 with 1 other product entry in Public Health Trace.

Responsible company: NATURE'S SUNSHINE PRODUCTS

Other recalls from NATURE'S SUNSHINE PRODUCTS

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.

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