Class IITerminated in FDA datasetApr 28, 2020

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

Check the codes ↓

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.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)

TypeCode / valueContext
UPC886790218302pplement, 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 ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.