Recall Record

Cincinnati, OH, United States

The Procter & Gamble Company recalls

5 recalls recorded since 2018, most recently on 1 February 2024. None are listed as ongoing. Status and classification are as published by the FDA.

Recalls5
Ongoing (FDA)0
Terminated or completed5
Class I (FDA)1

Terminated Class II Food

Recall started
1 February 2024
Terminated
21 November 2025
Reason
Illegible Label
Distribution
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
Initiated
Voluntary: Firm initiated
Recall number
F-0907-2024

Terminated Class II Food

Recall started
12 July 2022
Terminated
15 August 2024
Reason
Acidified/Low Acid dietary supplement with no approved process.
Distribution
Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Hampshire, New Jersey,
Initiated
Voluntary: Firm initiated
Recall numbers
F-1535-2022, F-1537-2022, F-1536-2022, F-1533-2022, F-1534-2022

Completed Class III Drugs

Recall started
8 July 2022
Reason
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
Distribution
Washington State
Initiated
Voluntary: Firm initiated
Recall number
D-1290-2022

Terminated Class II Food

Recall started
24 March 2022
Terminated
8 September 2022
Reason
Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.
Distribution
Product was sent to a 3rd party for destruction due to not meeting micro specs
Initiated
Voluntary: Firm initiated
Recall number
F-1012-2022

Terminated Class I, Class II Drugs

Recall started
23 November 2021
Terminated
1 October 2024
Reason
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Distribution
Nationwide USA and Puerto Rico, Canada, Guam, Northern Mariana Islands, American Samoa, Bhutan, Timor-Leste, Maldives, Fiji, US Virgin Islands, Trinidad, Peru, Saint Marteen, Bahamas, Costa Rica, Guatemala, Honduras, Panama, Belize, Santa Lucia, Aruba, Dominican Republic, Guyana
Initiated
Voluntary: Firm initiated
Recall numbers
D-0248-2024, D-0249-2024, D-0242-2024, D-0247-2024, D-0252-2024, D-0251-2024, D-0253-2024, D-0244-2024, D-0238-2024, D-0239-2024, D-0246-2024, D-0256-2024 and 7 more

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.