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RECALL RECORD — CLASS IIRecall closedF-1243-2013/FDA enforcement
Wynlife Healthcare, INC.·Dietary Supplements·May 31, 2011

Vegi-fiber Plus

What you need to know

Class II

  • What happened

    Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameWynlife Healthcare, INC.
Recalling firmWynlife Healthcare, INC.San Diego, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • PN 135
  • Lot #'s: 090336 and 100340
Distribution area
Nationwide

Nationwide distribution.

United States

Quantity affected210 boxes
Recall initiationFDA report date: March 27, 2013
FDA recall numberF-1243-2013

Beyond the headline

The recall, in context

Wynlife Healthcare, INC. initiated this supplements recall on May 31, 2011. The FDA enforcement report states: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents. The FDA report lists distribution as: Nationwide distribution.

The FDA enforcement report describes the reason as: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.

Vegi-fiber Plus was made or distributed by Wynlife Healthcare, INC. in San Diego, CA, United States. This page reflects FDA report F-1243-2013, dated March 27, 2013.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Vegi-fiber Plus recall?

Wynlife Healthcare, INC. recalled Vegi-fiber Plus in an FDA Class II enforcement action reported as F-1243-2013. Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Wynlife Healthcare, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1243-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Wynlife Healthcare, INC.

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Class II·

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All-in-one Probiotics, K12-bb12-lb3

Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.