Meta Psyllium Fiber Capsules (Procter & Gamble) – Illegible Label (2024)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.
Brand
The Procter & Gamble Company
Lot Codes / Batch Numbers
Lot Codes (100 count): 31661725G1, 32151725G1, 324211725G1, 32481725G1, 32611725G1, 32901725G1, 33131725G1, 33311725G1, 33411725G1, 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, 06/30/2026, 08/31/2026, 09/30/2026, 10/31/2026
Products Sold
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
The Procter & Gamble Company is recalling Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case. due to Illegible Label. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Illegible Label
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MS, MO, NV, NH, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VT, VA, WA, WI
Page updated: Jan 6, 2026