Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Food
Food & Beverages/Dietary Supplements

GPre and PreProtein Supplements Recalled for Bloated Packaging

Agency Publication Date: May 4, 2023
Share:
Sign in to monitor this recall

Summary

Novis PR, LLC dba Kramer Novis is recalling approximately 10,653 units of GPre and PreProtein liquid protein supplements because the packaging has been found to be bloated. The recall includes GPre Protein 16 oz bottles and PreProtein in both 30 mL pouches and 16 oz bottles with specific lot numbers 230118 and 230131. While no injuries or illnesses have been reported to date, bloating can indicate internal pressure or spoilage within the product container.

Risk

Bloated packaging in liquid dietary supplements typically signifies the presence of gases produced by microbial growth or chemical decomposition. Consuming products from such containers may lead to gastrointestinal illness or other health risks associated with spoiled protein.

What You Should Do

  1. This recall affects GPre Protein (16 oz bottles, UPC 52083633164, lot 230118), PreProtein (30 mL pouches, UPC 52083533105, lot 230118), and PreProtein (16 oz bottles, UPC 52083533167, lot 230131).
  2. Return the product to the place of purchase for a refund, throw it away, or contact Novis PR, LLC dba Kramer Novis for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

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: GPre Protein, Liquid predigested Protein, Dietary Supplement (16 oz)
Variants: 16 oz plastic bottle
UPC Codes:
52083633164
Lot Numbers:
230118
GTIN:
52083633164

Packed 12 units per case; Recall #: F-0810-2023

Product: PreProtein, Liquid Predigested Protein, Dietary Supplement (30 mL)
Variants: 30 mL pouch
UPC Codes:
52083533105
Lot Numbers:
230118
GTIN:
52083533105

Packed 200 units per case; Recall #: F-0811-2023

Product: PreProtein, Liquid Predigested Protein, Dietary Supplement (16 oz)
Variants: 16 oz bottle
UPC Codes:
52083533167
Lot Numbers:
230131
GTIN:
52083533167

Packed 12 units per case; Recall #: F-0812-2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92070
Status: Resolved
Manufacturer: Novis PR, LLC dba Kramer Novis
Manufactured In: United States
Units Affected: 3 products (6,034 units; 4106 units; 513 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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.