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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Dietary Supplements

Kramer Novis G-Pre Protein Recalled for Atypical Appearance and Odor

Agency Publication Date: October 12, 2022
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Summary

Novis PR, LLC is recalling 1,369 units of Kramer Novis G-Pre Protein, a cherry-flavored liquid predigested protein dietary supplement. The recall affects 16 fl oz bottles from Lot 080522 with an expiration date of August 2025. The product was found to have an unusual smell and atypical bubbles once the bottle was opened.

Risk

The product exhibits an atypical physical appearance and an unusual odor, indicating potential degradation or spoilage. No incidents or injuries have been reported to date.

What You Should Do

  1. This recall affects Kramer Novis G-Pre Protein (Liquid Predigested Protein), Cherry Flavor, sold in 16 fl oz (473 mL) bottles. The affected product is marked with Lot 080522 and an expiration date of 08/25.
  2. Check the bottle label for the lot number 080522 and the expiration date 08/25 to determine if your product is included in this recall.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. If you have further questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement (16 fl oz)
Variants: Cherry Flavor
Lot Numbers:
080522 (Exp 08/25)

Recall #: F-0037-2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90863
Status: Resolved
Manufacturer: Novis PR, LLC dba Kramer Novis
Manufactured In: United States
Units Affected: 1,369 units
Distributed To: Puerto Rico

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.