G-Supress DX — Class I drug recall D-0868-2023
Terminated recall by Novis PR, LLC dba Kramer Novis, reported 2023-06-07, distributed in PR. Product mix-up: incorrect product was found inside the G-Supress DX product carton.
| Recall number | D-0868-2023 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Novis PR, LLC dba Kramer Novis, San Juan, PR, United States |
| Recall initiated | 2023-04-20 |
| Classified | 2023-06-06 |
| Reported by FDA | 2023-06-07 |
| Terminated | 2024-09-13 |
| Distributed | PR |
| Quantity | 9,077 bottles |
| NDC | 52083-0655, 52083-0655-01 |
| Lot numbers | D20911, OCT/25 |
Product
G-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 52083-655-01
Reason for recall
Product mix-up: incorrect product was found inside the G-Supress DX product carton.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0868-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.