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
The exact product
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
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
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Original FDA code information
Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)
| 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
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.