Dr. Reddy's Laboratories, Inc. 2022-12-07 Health moderate FDA
Health · FDA · Recall #FDA-D-0073-2023
Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal… Recall
Issued December 7, 2022 · Dr. Reddy's Laboratories, Inc.
In December 2022, Dr. Reddy's Laboratories, Inc. recalled the Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal…, a moderate health recall reported by the FDA. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed dissolution specifications
What you should do
- 1 Stop using Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Dr. Reddy's Laboratories, Inc. to arrange your remedy. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy ():
Recall details
- Brand
- Dr. Reddy's Laboratories, Inc.
- Category
- Health
- Recall date
- December 7, 2022
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0073-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Dr. Reddy's Laboratories, Inc. has 17 recalls in our database, including 3 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.