The Procter & Gamble Company Recall: Illegible Label

🇺🇸 United States

1. February 1, 2024 - Recall initiated
2. February 28, 2024 - Reported by source
3. November 21, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0907-2024

Event ID

93916

Status

Terminated

Classification

Class II

Company

The Procter & Gamble Company

Product description

Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.

Quantity

21,428 cases TOTAL

Reason

Illegible Label

Recall initiation date

February 1, 2024

Report date

February 28, 2024

Classification date

Not published in this source record

Termination date

November 21, 2025

Distribution pattern

Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, Wisconsin

UPC, lot, and code information

Lot Codes (100 count): 31661725G1, 32151725G1, 324211725G1, 32481725G1, 32611725G1, 32901725G1, 33131725G1, 33311725G1, 33411725G1, 33451725G1 Product No (100 count): 80374550 Case UPC (100count): 10037000405143 Item UPC (100 count): 037000405146 Expiration Dates (100 count): 05/31/2026, 06/30/2026, 07/31/2026, 08/31/2026, 09/30/2026, 10/31/2026 Lot Codes(160 count): 31651725G2, 32171725G1, 32211725G1, 32411725G1, 32581725G, 32771725G1, 32911725G3, 32961725G1, 33171725G1, 33251725G2, 33451725G2 Product No. (160 count) 80374554 Case UPC (160 count): 10037000405112 Item UPC (16 count): 037000405115 Expiration Dates(for 160 count): 05/30/2026, 06/30/2026, 08/31/2026, 09/30/2026, 10/31/2026

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: The Procter & Gamble Company

Other recalls from The Procter & Gamble Company

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.

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