Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bottle.
Recalling firm: Glaxosmithkline Consumer Healthcare Holdings
Why it was recalled
Fiber prebiotic product potentially contaminated with small plastic pieces
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ProductBenefiber 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
UPC886790218302
FDA code information
Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)
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Full FDA record and distribution details
Original product description
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
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 886790218302 | pplement, 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 |
Recall details
- Recall number
- F-0951-2020
- Event ID
- 85554
- FDA status
- Terminated
- Initiated
- Apr 28, 2020
- Reported
- May 13, 2020
- Classified
- May 18, 2020
- Terminated
- Jun 1, 2021
- Quantity
- 170,340 bottles
- Location
- Warren, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
Distributed to the following US states: AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, and WI
FDA source record · F-0951-2020
Data updated September 16, 2026. View official FDA data ↗
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