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RECALL RECORD — CLASS IIIRecall closedF-0096-2017/FDA enforcement
Triceutical Inc./zhang·Dietary Supplements·Oct 10, 2014

Dietary Supplement Blue Rock Holistics Super Shield, 90 Vegetable Capsules, Distributed by: …

What you need to know

Class III

  • What happened

    Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. Current good manufacturing practice failures can affect product identity, strength, quality or purity.

  • 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 FDAFL, NY, PAMore supplements

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Product identification

Source: FDA FOOD

Brand nameTriceutical Inc./zhang
Recalling firmTriceutical Inc./zhangFarmingdale, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #: 120067, Best use before 04/2014
Distribution area
FLNYPA

*Domestic* - FL, NY, PA, *International*- China

United States, China

Quantity affected21, 825 bottles
Recall initiationFDA report date: October 26, 2016
FDA recall numberF-0096-2017

Beyond the headline

The recall, in context

Triceutical Inc./zhang initiated this supplements recall on October 10, 2014. The FDA enforcement report states: Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices. The FDA report lists distribution as: *Domestic* - FL, NY, PA, *International*- China.

The FDA enforcement report describes the reason as: Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.

Dietary Supplement Blue Rock Holistics Super Shield, 90 Vegetable Capsules, Distributed by: … was made or distributed by Triceutical Inc./zhang in Farmingdale, NY, United States. This page reflects FDA report F-0096-2017, dated October 26, 2016.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, current good manufacturing practice failures can affect product identity, strength, quality or purity.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 Dietary Supplement Blue Rock Holistics Super Shield, 90 Vegetable Capsules, Distributed by: … recall?

Triceutical Inc./zhang recalled Dietary Supplement Blue Rock Holistics Super Shield, 90 Vegetable Capsules, Distributed by: … in an FDA Class III enforcement action reported as F-0096-2017. Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Triceutical Inc./zhang?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0096-2017 and keep the packaging, lot code and proof of purchase if you have them.

Is the Triceutical Inc./zhang 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-0096-2017. 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

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