The Procter & Gamble Company Meta Psyllium Fiber Capsules packaged as 100 count or 160 recall — FDA F-0907-2024
Illegible Label
Overview of recall records associated with The Procter & Gamble Company, including dates, categories and classifications where available.
Classification mix: Class II: 19, Class I: 7, Class III: 1.
Illegible Label
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Chemical contamination: presence of benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Chemical contamination: presence of benzene
Chemical contamination: presence of benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Chemical contamination: presence of benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Chemical contamination: presence of benzene
Chemical contamination: presence of benzene
Chemical contamination: presence of benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Acidified/Low Acid dietary supplement with no approved process.
Acidified/Low Acid dietary supplement with no approved process.
Acidified/Low Acid dietary supplement with no approved process.
Acidified/Low Acid dietary supplement with no approved process.
This page summarizes recall records in which the official source identifies The Procter & Gamble Company as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.