Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0950-2020.
Fiber prebiotic product potentially contaminated with small plastic pieces
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0950-2020.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Glaxosmithkline Consumer Healthcare Holdings or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0950-2020.
Glaxosmithkline Consumer Healthcare Holdings
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Glaxosmithkline Consumer Healthcare Holdings Recall FAQ
Glaxosmithkline Consumer Healthcare Holdings is the subject of a supplements safety report: Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872. The notice was published on April 28, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 29,844 units are potentially affected.