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RECALL RECORD — CLASS IIRecall closedF-0999-2023/FDA enforcement
Entrinsic Health Solution INC·Dietary Supplements·May 25, 2023

Enterade Advanced Oncology Formula

What you need to know

Class II

  • What happened

    Potential for the product to develop mold and spoil.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

  • 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 FDAAL, AR, AZ, CA +43 moreMore supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameEntrinsic Health Solution INC
Recalling firmEntrinsic Health Solution INCNorwood, MA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot: OEV24122 and Exp: 8/29/24; Lot: OEV24222 and Exp: 8/30/24; Lot: OEV24322 and Exp: 8/31/24; Lot: OEV24422 and Exp: 9/1/24; Lot: OEV24522 and Exp: 9/2/24; Lot: OEV24922 and Exp: 9/6/24
  • Lot: OEV25022 and Exp: 9/7/24; Lot: OEV25122 and Exp: 9/8/24; Lot: OEV25222 and Exp: 9/9/24; Lot: OEV25522 and Exp: 9/12/24
Distribution area
ALARAZCACOCTDCDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNENJNMNVNYOHOKORPARISCSDTNTXUTVAVTWAWIWV

AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV

United States

Quantity affected43, 336 bottles
Recall initiationFDA report date: June 28, 2023
FDA recall numberF-0999-2023

Beyond the headline

The recall, in context

Entrinsic Health Solution INC initiated this supplements recall on May 25, 2023. The FDA enforcement report states: Potential for the product to develop mold and spoil. The FDA report lists distribution as: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV.

The FDA enforcement report describes the reason as: Potential for the product to develop mold and spoil.

Enterade Advanced Oncology Formula was made or distributed by Entrinsic Health Solution INC in Norwood, MA, United States. This page reflects FDA report F-0999-2023, dated June 28, 2023.

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, visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

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

Mold contamination

Symptoms to watch for

Eating a moldy product may cause nausea, vomiting, diarrhea or allergic reactions. Do not intentionally inspect, smell or taste a suspect product.

Higher-risk groups

People with mold allergies, asthma, a weakened immune system, pregnant people and young children should be especially cautious.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Visible mold can indicate a moisture, packaging or temperature failure.

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 Enterade Advanced Oncology Formula recall?

Entrinsic Health Solution INC recalled Enterade Advanced Oncology Formula in an FDA Class II enforcement action reported as F-0999-2023. Potential for the product to develop mold and spoil.

What are the symptoms of Mold contamination exposure?

Eating a moldy product may cause nausea, vomiting, diarrhea or allergic reactions. Do not intentionally inspect, smell or taste a suspect product.

Who is most at risk from Mold contamination?

People with mold allergies, asthma, a weakened immune system, pregnant people and young children should be especially cautious.

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 affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

How do I get a refund from Entrinsic Health Solution INC?

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-0999-2023 and keep the packaging, lot code and proof of purchase if you have them.

Is the Entrinsic Health Solution 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-0999-2023. 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

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