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
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
- Recalling firm
- Glaxosmithkline Consumer Healthcare Holdings, Warren, NJ
- Brand
- Benefiber Prebiotic
- 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 2020 | Recall initiated by company | |
| 13 May 2020 | Published in enforcement report | +15 days |
| 18 May 2020 | Classified 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 85554This product is part of a recall event; the main page for the event is Benefiber Healthy Shape Prebiotic Fiber Supplement recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Benefiber Healthy Shape Prebiotic Fiber Supplement recalledBenefiber Healthy | Glaxosmithkline Consumer Healthcare Holdings | Foreign Material | 25 states |
More recalls from Glaxosmithkline Consumer Healthcare Holdings
All 26| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalled | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalled | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalledTums | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalledTums | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalledTums | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
Other Probiotics recalls
All 72| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Neuro Nourish dietary supplement;-1 Prebiotic, Probiotic recalledNeuro Nourish | Sensory Supplement | Other | Nationwide |
| Food | CLASS I | SunBiotics Activated Almonds Infused with Probiotics recalledSunBiotics Activated | Windy City Organics | Salmonella | 7 states |
| Food | CLASS II | Biostime Kids Calm & Sleep Support Fruity Bites Probiotics recalledBiostime Kids | Health and Happiness (H&H) | Foreign Material | CA, IL, TN |
| Food | CLASS II | ZOE Daily 30+ Prebiotic blend recalled by Zoe USZoe | Zoe US | Foreign Material | 26 states |
| Food | CLASS I | Mt. Capra Goat Milk Formula Recipe Kit recalled by Healthwest MineralsMt. Capra | Healthwest Minerals | Packaging Defects | Nationwide |