Recall Register

Food, drugs, devices › Firms

Novis PR, LLC dba Kramer Novis

FDA recalling firm · 3 enforcement events · 5 product records · 2022–2023 · PR

Novis PR, LLC dba Kramer Novis has 3 FDA enforcement events on this register (5 product records) between 2022 and 2023: 2 food and 1 drug; the busiest year was 2023 with 2.

33% of its events are Class I; the most common class is Class I (1). 0 events are listed as ongoing; the recalling firm's address is in PR.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
20 Apr 2023G-Supress DX (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl) Pediatric Drops Cough Suppressant Expectorant Nasal Decongestant, Cherry Flavor Sugar & Alcohol Free, packaged in a bottle Net Content: 30 mL (1 oz.) further packaged in a carton, Manufactured in the USA for Kramer Novis, San Juan, PR 00917, NDC…DrugClass I1Terminated
27 Mar 2023GPre Protein, Liquid predigested Protein, Dietary Supplement, Nt Wt. 16 oz, plastic bottle packed 12 units of 16 oz in 1 case.FoodClass II3Terminated
25 Aug 2022G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents 16 fl oz (473 mL), Kramer NovisFoodClass III1Terminated

By type and class

Food2
Drug1
Class I1
Class II1
Class III1

Class I: 33% of this firm's events; 18% of all events on the register.

Events by year

22
23
24
25
26
Enforcement events for Novis PR, LLC dba Kramer Novis by year initiated.

Questions and answers

How many FDA recalls has Novis PR, LLC dba Kramer Novis had?

3 enforcement events (5 product records) on this register, 2022–2023: 2 food, 1 drug.

Are any Novis PR, LLC dba Kramer Novis recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Novis PR, LLC dba Kramer Novis recalls?

1 Class I, 1 Class II, 1 Class III. 33% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.