RecallRadar

FDA Drug recall D-0422-2015

Haloperidol Decanoate Injection, 50 mg/mL, For Intra Muscular Use Only, 1 mL single dose vials (NDC 67457-410-00) packaged in cartons of te…

On 2015-04-01 the FDA classified a Class II recall of Haloperidol Decanoate Injection, 50 mg/mL, For Intra Muscular Use Only, 1 mL single dose vials (NDC 67457-410-00) packaged in cartons of te… by Mylan Institutional, citing lack of Assurance of Sterility; due to leaking vials.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0422-2015
ClassificationClass II
Statusterminated
Initiated2015-02-18
Published2015-04-01
Last updated2026-09-13 11:51 UTC
CompanyMylan Institutional
DistributionUS

Product

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

Lack of Assurance of Sterility; due to leaking vials

Identifiers

ndc67457-410-00
ndc67457-410-13
ndc67457-409-00
ndc67457-409-13
code_infoLot 7602368, Exp 7/16; Lot 7602369, Exp 7/16

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0422-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.