PlainRecalls
FDA Drug Moderate Class II Terminated

Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0173-10

Reported: August 14, 2019 Initiated: June 19, 2019 #D-1634-2019

Product Description

Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0173-10

Reason for Recall

Crystallization

Details

Recalling Firm
RXQ Compounding LLC
Units Affected
N/A
Distribution
Nationwide USA
Location
Athens, OH

Frequently Asked Questions

What product was recalled?
Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0173-10. Recalled by RXQ Compounding LLC. Units affected: N/A.
Why was this product recalled?
Crystallization
Which agency issued this recall?
This recall was issued by the FDA Drug on August 14, 2019. Severity: Moderate. Recall number: D-1634-2019.