PlainRecalls
FDA Drug Moderate Class II Terminated

Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807, NDC 70121-1390-1

Reported: April 4, 2018 Initiated: December 15, 2017 #D-0610-2018

Product Description

Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807, NDC 70121-1390-1

Reason for Recall

Presence of particulate matter

Details

Recalling Firm
Amneal Pharmaceuticals
Units Affected
12,584 vials
Distribution
U.S.A Nationwide
Location
Brookhaven, NY

Frequently Asked Questions

What product was recalled?
Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807, NDC 70121-1390-1. Recalled by Amneal Pharmaceuticals. Units affected: 12,584 vials.
Why was this product recalled?
Presence of particulate matter
Which agency issued this recall?
This recall was issued by the FDA Drug on April 4, 2018. Severity: Moderate. Recall number: D-0610-2018.