LowClass IIITerminated

FDA Food recall · Reported October 19, 2022

G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents 16 fl oz (473 mL), Kramer Novis

Q: Which agency issued this recall?

This recall was issued by the FDA Food on October 19, 2022. Severity: Low. Recall number: F-0037-2023.

Q: Where was the recalled product distributed?

Distribution: Domestic distribution only (Puerto Rico)..

Q: What are the health risks of consuming a recalled food product?

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present.

Recall #: F-0037-2023
Affected scope: 1,369 units
Initiated: August 25, 2022

Compiled from official public sources by the publisher. · Updated September 2026

Verify with FDA Food →

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Novis Pr, LLC dba Kramer Novis recalled G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents… - a low-severity action.

G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents… was recalled by Novis Pr, LLC dba Kramer Novis in October 19, 2022. Reason: Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypic…. Check the official notice for the remedy. Verify recall #F-0037-2023 with the FDA Food before acting.

The recall

Novis Pr, LLC dba Kramer Novis issued this low-severity FDA Food recall-Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypic….

Low
severity level: 1K units
affected scope: Class III
classification: October 19, 2022
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0037-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents 16 fl oz (473 mL), Kramer Novis

Reason for recall

Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present.

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Low (Class III)
Status	Terminated
Recall number	F-0037-2023
Date reported	October 19, 2022
Date initiated	August 25, 2022
Recalling firm	Novis Pr, LLC dba Kramer Novis
Firm location	San Juan, PR
Affected scope	1,369 units
Distribution	Domestic distribution only (Puerto Rico).

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

1,369 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall

Multi-state (10K – 100K units) -

Large-scale (100K – 1M units) -

Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-0037-2023) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents 16 fl oz (473 mL), Kramer Novis. Recalled by Novis Pr, LLC dba Kramer Novis. Units affected: 1,369 units.

Why was this product recalled? ▼

Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present.

Which agency issued this recall? ▼

This recall was issued by the FDA Food on October 19, 2022. Severity: Low. Recall number: F-0037-2023.

Where was the recalled product distributed? ▼

Distribution: Domestic distribution only (Puerto Rico)..

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Low), closest by report date among other firms and states.

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Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported October 19, 2022. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026