Alkermes recalls

Alkermes has 4 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 9 Oct 2019. The most frequent reason is packaging defects.

Total recalls4since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 9 Oct 2019

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 4 100%Class III 0 0%

Why alkermes is recalled

Product types

Injectable & IV Drugs4100%

By year

2019250%
2014125%
2013125%

All alkermes recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
9 Oct 2019Drug	CLASS II	Vivitrol (naltrexone for extended-release injectable recalledVivitrol	Alkermes	Packaging Defects	Nationwide
4 Sep 2019Drug	CLASS II	Vivitrol (naltrexone for extended-release injectable recalledVivitrol	Alkermes	Packaging Defects	Nationwide
3 Sep 2014Drug	CLASS II	Vivitrol (naltrexone for extended-release injectable suspension) recalledVivitrol	Alkermes	Other	Nationwide
31 Jul 2013Drug	CLASS II	Vivitrol (naltrexone for extended-release injectable recalledVivitrol	Alkermes	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.