PlainRecalls
FDA Drug Moderate Class II Terminated

Haloperidol Decanoate Injection, 50 mg/mL, For Intra Muscular Use Only, 1 mL single dose vials (NDC 67457-410-00) packaged in cartons of ten (NDC 67457-410-13), Rx only, Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103

Reported: April 1, 2015 Initiated: February 18, 2015 #D-0422-2015

Product Description

Haloperidol Decanoate Injection, 50 mg/mL, For Intra Muscular Use Only, 1 mL single dose vials (NDC 67457-410-00) packaged in cartons of ten (NDC 67457-410-13), Rx only, Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103

Reason for Recall

Lack of Assurance of Sterility; due to leaking vials

Details

Recalling Firm
Mylan Institutional LLC
Units Affected
2,523 cartons (25,936 vials)
Distribution
Nationwide and Puerto Rico
Location
Rockford, IL

Frequently Asked Questions

What product was recalled?
Haloperidol Decanoate Injection, 50 mg/mL, For Intra Muscular Use Only, 1 mL single dose vials (NDC 67457-410-00) packaged in cartons of ten (NDC 67457-410-13), Rx only, Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103. Recalled by Mylan Institutional LLC. Units affected: 2,523 cartons (25,936 vials).
Why was this product recalled?
Lack of Assurance of Sterility; due to leaking vials
Which agency issued this recall?
This recall was issued by the FDA Drug on April 1, 2015. Severity: Moderate. Recall number: D-0422-2015.