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Class II: temporary or reversible health riskTerminated

Glaxosmithkline Consumer Healthcare Holdings Benefiber Prebiotic Fiber Supplement Recall

Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt

Glaxosmithkline Consumer Healthcare Holdings · Warren, NJ

Risk level
Class II
Reported by FDA
May 13, 2020
Recall ID
F-0951-2020
Check your lot numberHow we source this data

Summary

Glaxosmithkline Consumer Healthcare Holdings recalled Benefiber Prebiotic Fiber Supplement starting Apr 28, 2020. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0951-2020 on May 13, 2020. Reason: Fiber prebiotic product potentially contaminated with small plastic pieces. Status: Terminated.

Why it was recalled

Fiber prebiotic product potentially contaminated with small plastic pieces

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

Lot numbers, UPCs & expiration codes

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

Where it was 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 to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0951-2020
Classification
Class II
Status
Terminated
Recall initiated
Apr 28, 2020
FDA report date
May 13, 2020
Quantity
170,340 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Glaxosmithkline Consumer Healthcare Holdings

Original FDA data

Every field from FDA enforcement report F-0951-2020, exactly as published.

Show all FDA fields
City
Warren
State
NJ
Status
Terminated
Country
United States
Event ID
85554
Address
184 Liberty Corner Rd
Code information
Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)
Postal code
07059-6796
Report date
May 13, 2020
Product type
Food
Recall number
F-0951-2020
Classification
Class II
Recalling firm
Glaxosmithkline Consumer Healthcare Holdings
Product quantity
170,340 bottles
Termination date
Jun 1, 2021
Reason for recall
Fiber prebiotic product potentially contaminated with small plastic pieces
Voluntary / mandated
Voluntary: Firm initiated
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
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
Recall initiation date
Apr 28, 2020
Initial firm notification
Press Release
Center classification date
May 18, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0951-2020, published May 13, 2020. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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