G-PREPROTEIN Liquid Dietary Supplement Recalled for Quality and Appearance Issues
Novis PR, LLC recalled G-PREPROTEIN Liquid Dietary Supplement due to atypical bottle appearance, unusual odor, and atypical bubbles when opened. The recall affects 1,369 units distributed in Puerto Rico.
The agency’s classification
FDA (Food): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class III classification with no reported illnesses or injuries, combined with signs of possible spoilage (unusual odor and bubbles) but no confirmed pathogen identified, classifies this as a low-risk precautionary recall.
Plain-English summary
G-PREPROTEIN is a liquid dietary supplement marketed as a predigested protein product in cherry flavor, supplied in 16 fl oz (473 mL) bottles. The product is manufactured by Novis PR, LLC, operating as Kramer Novis.
The recall was initiated due to physical quality concerns. Affected bottles showed atypical appearance. Upon opening, unusual odor and atypical bubbles were observed, which may indicate spoilage or product degradation.
The recall affects approximately 1,369 units distributed exclusively in Puerto Rico. Affected units are identified as Lot 080522 with an expiration date of August 2025.
Consumers possessing this product should discontinue use and discard it. Consumers who have consumed the product and experience any adverse effects should consult a healthcare provider and may report the issue to the FDA.
The recalled product
- Product
- G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents 16 fl oz (473 mL), Kramer Novis
- Manufacturer
- Novis PR, LLC dba Kramer Novis
- Category
- Food — Dietary Supplement
- Affected units
- 1,369
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot 080522
- Exp Date 08/25
Distribution
Distributed in 1 state:
Related recalls
Same manufacturer · Novis PR, LLC dba Kramer Novis
See all →- SeverePediatric Cough Suppressant G-SUPRESS DX Recalled Due to Product Mix-Up
FDA (Drugs) · 2023-06-07
- HighPreProtein Dietary Supplement Bottles Recalled for Packaging Defect
FDA (Food) · 2023-05-10
- HighDietary Supplement Protein Bottles Recalled for Bloated Packaging
FDA (Food) · 2023-05-10
- ModeratePreProtein Liquid Dietary Supplement Recalled for Bloated Bottles
FDA (Food) · 2023-05-10
Same hazard · contamination
See all →- SevereAVID Medical Recalls Halyard Anterior Hip Packs Due to Sterilization Error
FDA (Devices) · 2026-10-28
- SevereFDA Recalls Argatroban Injection Vials Due to Particulate Matter
FDA (Drugs) · 2026-10-28
- SevereGreiner VACUETTE Blood Collection Tubes Recalled for EDTA Contamination
FDA (Devices) · 2026-10-28
- SevereEthicon Recalls Silk Surgical Sutures Packaged with Alcohol-Based Fluid
FDA (Devices) · 2026-10-21
- ModerateBioFire Joint Infection Panel Recalled for Potential Contamination
FDA (Devices) · 2026-10-21
Similar recalls
- ModeratePreProtein Liquid Dietary Supplement Recalled for Bloated Bottles
FDA (Food) · 2023-05-10
- HighPreProtein Dietary Supplement Bottles Recalled for Packaging Defect
FDA (Food) · 2023-05-10
- HighDietary Supplement Protein Bottles Recalled for Bloated Packaging
FDA (Food) · 2023-05-10
- SeverePediatric Cough Suppressant G-SUPRESS DX Recalled Due to Product Mix-Up
FDA (Drugs) · 2023-06-07
- ModerateNeuro Nourish dietary supplement recalled over premature lipid oxidation
FDA (Food) · 2026-06-17
- HighBenefiber Prebiotic Fiber Supplement Recalled for Potential Plastic Contamination
FDA (Food) · 2020-05-13