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

Benefiber Healthy Shape Prebiotic Fiber Supplement recalled

Glaxosmithkline Consumer Healthcare Holdings is recalling Benefiber Healthy Shape 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 codesLot: MP8B (EXP Sep2021)
Quantity recalled29,844 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-0950-2020
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 Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872

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?

Lot: MP8B (EXP Sep2021)

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
ReportedClassRecallCompanyReasonWhere
CLASS IIBenefiber Prebiotic Fiber Supplement recalledBenefiber PrebioticGlaxosmithkline Consumer Healthcare HoldingsForeign Material25 states

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