Severity
Low
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
Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
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 FDA Food action (record #F-0037-2023) was formally reported on October 19, 2022, with the manufacturer initiating the action on August 25, 2022. It is classified under Low severity (Class III), with a current status of Terminated. Novis Pr, LLC dba Kramer Novis is listed as the recalling firm, operating out of San Juan, PR. Federal records list the affected scope as 1,369 units.
The documented reason for this recall is: Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present. Distribution data in the federal record shows the product reached: Domestic distribution only (Puerto Rico).. Distribution scope 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.
Affected scope
1,369 units
Related Recalls
6
0 from same agency
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
| 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.
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)..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0037-2023) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported October 19, 2022. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.