RecallRadar

FDA Food recall F-0951-2020

Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bottle

On 2020-05-13 the FDA classified a Class II recall of Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bottle by Glaxosmithkline Consumer Healthcare Holdings, citing fiber prebiotic product potentially contaminated with small plastic pieces.

Read the official FDA Food notice

AgencyFDA Food
Recall numberF-0951-2020
ClassificationClass II
Statusterminated
Initiated2020-04-28
Published2020-05-13
Last updated2026-09-13 11:50 UTC
CompanyGlaxosmithkline Consumer Healthcare Holdings
DistributionAR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, WI

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

Reason

Fiber prebiotic product potentially contaminated with small plastic pieces

Identifiers

upc886790218302
upc8886790211907
code_infoLots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0951-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.