Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.
Summary
The FDA issued a Class II for Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 by The Procter & Gamble Company. Reason: Illegible Label.
Details
Source
Food Recall
External ID
F-0907-2024
Action Date
2024-02-28
Status
Terminated
Category
food
Product Description
Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.
Lot/Code Info: 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
Quantity Affected: 21,428 cases TOTAL
Reason for Recall
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, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, Wisconsin
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-01
Company
Cincinnati, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Procter & Gamble Company has 27 FDA actions in our database, including 27 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (The Procter & Gamble Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Procter & Gamble Company have FDA actions?
The Procter & Gamble Company has 27 FDA actions in our database, including 27 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0907-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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