Novis PR, LLC dba Kramer Novis 2023-06-07 Health critical FDA
Health · FDA · Recall #FDA-D-0868-2023
G-Supress DX (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl) Pediatric Drops Cough… Recall
Issued June 7, 2023 · Novis PR, LLC dba Kramer Novis
In June 2023, Novis PR, LLC dba Kramer Novis recalled the G-Supress DX (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl) Pediatric Drops Cough…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Product mix-up: incorrect product was found inside the G-Supress DX product carton.
What you should do
- 1 Stop using G-Supress DX (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl) Pediatric Drops Cough… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Novis PR, LLC dba Kramer Novis to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Novis PR, LLC dba Kramer Novis
- Category
- Health
- Recall date
- June 7, 2023
- Units affected
- Not reported
- Sold at
- Puerto Rico
- Recall number
- FDA-D-0868-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Novis PR, LLC dba Kramer Novis has 2 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.