Procter & Gamble Meta Psyllium Fiber Capsules: Illegible Label Hazard
Procter & Gamble recalls Meta Psyllium Fiber Capsules with illegible labels that could lead to incorrect dosage. Affected products include 100-count and 160-count PET bottles sold in cases of 12.
Lower-risk recall
Illegible Label
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What happened, in plain English
Procter & Gamble is recalling Meta Psyllium Fiber Capsules due to illegible labels that may cause users to take the wrong dose. This could lead to improper fiber intake and potential health issues. Read more at govinfonow.com/recall/9681-procter-gamble-meta-psyllium-fiber-capsules-illegible-label-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/9681-procter-gamble-meta-psyllium-fiber-capsules-illegible-label-hazard · Updated August 18, 2026 · FDA enforcement record: FDA #F-0907-2024
Cite this page
“Procter & Gamble Meta Psyllium Fiber Capsules: Illegible Label Hazard.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/9681-procter-gamble-meta-psyllium-fiber-capsules-illegible-label-hazard. Based on FDA recall #F-0907-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0907-2024%22&limit=1).
Why it’s dangerous
The labels on these capsules are illegible, which means users might not be able to see the correct dosage instructions. This could result in taking too much or too little fiber, potentially causing digestive issues or other health problems.
Who’s affected
People who purchased Meta Psyllium Fiber Capsules in 100-count or 160-count PET bottles with specific lot codes and expiration dates listed in the recall notice. Those most at risk are individuals who rely on precise dosing for their fiber intake.
How to tell if you have this one
Check for lot codes and expiration dates listed in the recall notice: 100-count bottles have lot codes like 31661725G1 and expire by 10/31/2026, while 160-count bottles have lot codes like 31651725G2 and expire by 10/31/2026.
- Brand
Procter & Gamble- Category
Food
What to do — step by step
Check Product Labels
Look for the lot codes and expiration dates listed in the recall notice to determine if your product is affected.
Where it went and when
Where it was distributed
Distributed in 41 states.
FDA 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…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: 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.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0907-2024 (February 1, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0907-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.