Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported May 13, 2020
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
Fiber prebiotic product potentially contaminated with small plastic pieces
Glaxosmithkline Consumer Healthcare Holdings recalled Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17… - a moderate-severity action.
Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17… was recalled by Glaxosmithkline Consumer Healthcare Holdings in May 13, 2020. Reason: Fiber prebiotic product potentially contaminated with small plastic pieces. Check the official notice for the remedy. Verify recall #F-0951-2020 with the FDA Food before acting.
The recall
Glaxosmithkline Consumer Healthcare Holdings issued this moderate-severity FDA Food recall-Fiber prebiotic product potentially contaminated with small plastic pieces.
- Moderate
- severity level
- Class II
- classification
- May 13, 2020
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0951-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0951-2020) was formally reported on May 13, 2020, with the manufacturer initiating the action on April 28, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Glaxosmithkline Consumer Healthcare Holdings is listed as the recalling firm, operating out of Warren, NJ. Federal records list the affected scope as 170,340 bottles.
The documented reason for this recall is: Fiber prebiotic product potentially contaminated with small plastic pieces Distribution data in the federal record shows the product reached: 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. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
170,340 bottles
Related Recalls
6
0 from same agency
Product description
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 for recall
Fiber prebiotic product potentially contaminated with small plastic pieces
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0951-2020 |
| Date reported | May 13, 2020 |
| Date initiated | April 28, 2020 |
| Recalling firm | Glaxosmithkline Consumer Healthcare Holdings |
| Firm location | Warren, NJ |
| Affected scope | 170,340 bottles |
| Distribution | 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 |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0951-2020) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Glaxosmithkline Consumer Healthcare Holdings. Units affected: 170,340 bottles.
Why was this product recalled? ▼
Fiber prebiotic product potentially contaminated with small plastic pieces
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 13, 2020. Severity: Moderate. Recall number: F-0951-2020.
Where was the recalled product distributed? ▼
Distribution: 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.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0951-2020) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
CPSC Moderate
AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards fo…
Xishentang Dongguan Trading Co, Ltd., dba Pretty-Life, of China · 2026-07-02
CPSC Moderate
Diamond Wipes International Recalls CVS Health Medicated Hemorrhoidal Wipes Due to Risk of Serious Injury or Death from…
Diamond Wipes International, Inc. of Chino, California · 2026-07-02
CPSC Moderate
Junpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; V…
· 2026-07-02
CPSC Moderate
Target Recalls Gigglescape™ Under the Sea Popping Toy Due to Choking Hazard
· 2026-07-02
CPSC Moderate
Vevor Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory …
Sanven Technology Ltd., dba Vevor, of Rancho Cucamonga, California · 2026-07-02
Compare this recall with AMASKY Nursing Pillows Recalled Due to Risk of Serious Inju… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported May 13, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.