RECALL RECORD — CLASS IIRecall closedF-0812-2023/FDA enforcement

Preprotein, Liquid Predigested Protein, Dietary Supplement, Nt WT

What you need to know

Class II
  • What happened

    Bloated Protein Bottle

  • 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 FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameNovis Pr, LLC Dba Kramer Novis
Recalling firmNovis Pr, LLC Dba Kramer NovisSan Juan, PR, United States
UPC / barcodes
52083533167
Lot / date codes
  • lot 230131 UPC Code:52083533167
Distribution area

Domestic distribution only.

United States

Quantity affected513 units
Recall initiationFDA report date: May 10, 2023
FDA recall numberF-0812-2023

Beyond the headline

The recall, in context

Novis Pr, LLC Dba Kramer Novis initiated this supplements recall on March 27, 2023. The FDA enforcement report states: Bloated Protein Bottle. The FDA report lists distribution as: Domestic distribution only.

The FDA enforcement report describes the reason as: Bloated Protein Bottle

Preprotein, Liquid Predigested Protein, Dietary Supplement, Nt WT was made or distributed by Novis Pr, LLC Dba Kramer Novis in San Juan, PR, United States. This page reflects FDA report F-0812-2023, dated May 10, 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, 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 UPC and lot code 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 Preprotein, Liquid Predigested Protein, Dietary Supplement, Nt WT recall?

Novis Pr, LLC Dba Kramer Novis recalled Preprotein, Liquid Predigested Protein, Dietary Supplement, Nt WT in an FDA Class II enforcement action reported as F-0812-2023. Bloated Protein Bottle

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 Novis Pr, LLC Dba Kramer Novis 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-0812-2023. 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

Brand history

More recalls by Novis Pr, LLC Dba Kramer Novis

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