PlainRecalls
FDA Drug Moderate Class II Completed

Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation or Injection, Must be Diluted, Manufactured by: The Ritedose Corporation Columbia, SC 29203 for Ritedose Pharmaceuticals, LLC Columbia, SC 29203, NDC 76204-025-96.

Reported: August 9, 2023 Initiated: July 21, 2023 #D-0946-2023

Product Description

Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation or Injection, Must be Diluted, Manufactured by: The Ritedose Corporation Columbia, SC 29203 for Ritedose Pharmaceuticals, LLC Columbia, SC 29203, NDC 76204-025-96.

Reason for Recall

CGMP deviation: product released prior to supplier approval.

Details

Recalling Firm
The Ritedose Corporation
Units Affected
44 cartons
Distribution
Nationwide in the US
Location
Columbia, SC

Frequently Asked Questions

What product was recalled?
Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation or Injection, Must be Diluted, Manufactured by: The Ritedose Corporation Columbia, SC 29203 for Ritedose Pharmaceuticals, LLC Columbia, SC 29203, NDC 76204-025-96.. Recalled by The Ritedose Corporation. Units affected: 44 cartons.
Why was this product recalled?
CGMP deviation: product released prior to supplier approval.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 9, 2023. Severity: Moderate. Recall number: D-0946-2023.