PlainRecalls
FDA Drug Low Class III Terminated

Levetiracetam Injection, 500 mg/5mL, 10 single-use 5 mL vials, Rx only, Manufactured by: Agile Specialties Private Limited Pilot No. 14, Sipcot II, Hosur-635 109 Tamil Nadu, India, Manufactured for: X-Gen Pharmaceuticals, Inc. Big Flats, NY 14814, NDC 39822-4000-1

Reported: November 27, 2019 Initiated: October 11, 2019 #D-0519-2020

Product Description

Levetiracetam Injection, 500 mg/5mL, 10 single-use 5 mL vials, Rx only, Manufactured by: Agile Specialties Private Limited Pilot No. 14, Sipcot II, Hosur-635 109 Tamil Nadu, India, Manufactured for: X-Gen Pharmaceuticals, Inc. Big Flats, NY 14814, NDC 39822-4000-1

Reason for Recall

Labeling: Incorrect or Missing Package Insert - the incorrect package insert version was attached.

Details

Units Affected
25120 vials
Distribution
U.S.A. Nationwide
Location
Horseheads, NY

Frequently Asked Questions

What product was recalled?
Levetiracetam Injection, 500 mg/5mL, 10 single-use 5 mL vials, Rx only, Manufactured by: Agile Specialties Private Limited Pilot No. 14, Sipcot II, Hosur-635 109 Tamil Nadu, India, Manufactured for: X-Gen Pharmaceuticals, Inc. Big Flats, NY 14814, NDC 39822-4000-1. Recalled by X-Gen Pharmaceuticals Inc.. Units affected: 25120 vials.
Why was this product recalled?
Labeling: Incorrect or Missing Package Insert - the incorrect package insert version was attached.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 27, 2019. Severity: Low. Recall number: D-0519-2020.