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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
Fiber prebiotic product potentially contaminated with small plastic pieces
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bottle. UPC 886790218302 and 2) Net Wt. 760 g bottle UPC 8886790211907 | 886790218302 | 170,340 bottles | Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021) |
This recall shares FDA event ID 85554 with 1 other product entry in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
Responsible company: Glaxosmithkline Consumer Healthcare Holdings
FDA Recall Terminated Historical recordClass II
FDA Recall Terminated Historical recordClass II
FDA Recall Terminated Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Arkansas | 1 |
| California | 1 |
| Florida | 1 |
| Hawaii | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Carolina | 1 |
| Texas | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
