Key Takeaway

Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872 by Glaxosmithkline Consumer Healthcare Holdings was recalled on April 28, 2020. The hazard: Fiber prebiotic product potentially contaminated with small plastic pieces

FDA Food Class II Terminated

Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872

Recalled: April 28, 2020 ~29,844 bottles units affected F-0950-2020

Description

Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872

Hazard / Reason

Fiber prebiotic product potentially contaminated with small plastic pieces

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872

Food

Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872

Food

Company Information

Glaxosmithkline Consumer Healthcare Holdings

Warren, NJ, United States

View all 16 recalls by Glaxosmithkline Consumer Healthcare Holdings →

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

Related Recalls

FDA Drug Class II

Childrens Dimetapp Cold & Cough, For ages 6 yrs. & over, 8 FL OZ. bottle, (237 mL), Distributed by: Pfizer Madison, NJ 07940, Made in Canada, UPC: 60300312234196, NDC: 0031-2234-19.

June 16, 2020
FDA Drug Class II

Childrens Robitussin Honey Cough and Chest Congestion DM, dextromethorphan (cough suppressant), guaifenesin (expectorant), 4 FL OZ. bottle (118 mL), Distributed by: Pfizer, Madison, NJ 07940 USA, UPC:

June 16, 2020
FDA Drug Class II

Gaviscon Extra Strength Liquid Antacid Extra Strength Cherry, 12 FL OZ. (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0574-41

May 28, 2020
FDA Drug Class II

Gaviscon Liquid Antacid Extra Strength, Cool Mint, 12 FL OZ (355 mL) single pack and twin pack, Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0095-41

May 28, 2020
FDA Drug Class II

Gaviscon Regular Strength Liquid Antacid Cool Mint, 12 FL OZ (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0094-41

May 28, 2020
FDA Drug Class II

Gaviscon Regular Strength Liquid Antacid Cool Mint, 6 FL OZ (177 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0094-42

May 28, 2020

Frequently Asked Questions

Is this recall still active?

Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.

How do I check if my product is affected?

Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.

What remedy is available for this recall?

Check the remedy section above or contact the manufacturer directly for current remedy options.

Where can I find the original recall notice?

This recall was issued by FDA Food. Visit the agency's official website for the original notice.

Data sourced from FDA Food Enforcement. Recall information may not reflect the most current status. RecallDex is not affiliated with any US government agency. Contact the manufacturer or relevant agency for the latest information.