F-0951-2020 Class II Terminated

Recalled by Glaxosmithkline Consumer Healthcare Holdings — Warren, NJ

FDA food recall F-0951-2020 was initiated by Glaxosmithkline Consumer Healthcare Holdings on Apr 28, 2020 and is designated Class II. Reason for recall: Fiber prebiotic product potentially contaminated with small plastic pieces The recall status is terminated (terminated Jun 1, 2021). Affected quantity: 170,340 bottles.

Recall details

Product Type
Food
Report Date
May 13, 2020
Initiation Date
Apr 28, 2020
Termination Date
Jun 1, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
170,340 bottles

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

Distribution pattern

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

Code information

Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0951-2020
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 15, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for F-0951-2020. Report a data issue: hello@regdatalab.com.