CLASS II Food recall · Reported 13 May 2020 · FDA Enforcement Report

Benefiber Prebiotic Fiber Supplement recalled

Glaxosmithkline Consumer Healthcare Holdings is recalling Benefiber Prebiotic Fiber Supplement, distributed in 25 states. The recall was initiated on 28 Apr 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)
Quantity recalled170,340 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0951-2020
FDA event ID
85554
Classification
Class II
Status
Terminated
Recall initiated
28 Apr 2020
FDA classified
18 May 2020
Reported
13 May 2020
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Foreign Material
Product category
Probiotics

Timeline

28 Apr 2020Recall initiated by company
13 May 2020Published in enforcement report+15 days
18 May 2020Classified by FDA+5 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Fiber prebiotic product potentially contaminated with small plastic pieces

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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

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

ArkansasCaliforniaFloridaHawaiiIdahoIllinoisLouisianaMassachusettsMaineMichiganMinnesotaMissouriNorth CarolinaNebraskaNew JerseyNew YorkOhioOregonPennsylvaniaRhode Island

Questions about this recall

Why was it recalled?

Fiber prebiotic product potentially contaminated with small plastic pieces

Which lots are affected?

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

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 85554

This product is part of a recall event; the main page for the event is Benefiber Healthy Shape Prebiotic Fiber Supplement recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIBenefiber Healthy Shape Prebiotic Fiber Supplement recalledBenefiber HealthyGlaxosmithkline Consumer Healthcare HoldingsForeign Material25 states

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