PlainRecalls
FDA Drug Critical Class I Terminated

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

Reported: June 7, 2023 Initiated: April 20, 2023 #D-0868-2023

Product Description

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.

Details

Units Affected
9077 bottles
Distribution
Puerto Rico
Location
San Juan, PR

Frequently Asked Questions

What product was recalled?
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. Recalled by Novis PR, LLC dba Kramer Novis. Units affected: 9077 bottles.
Why was this product recalled?
Product mix-up: incorrect product was found inside the G-Supress DX product carton.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 7, 2023. Severity: Critical. Recall number: D-0868-2023.