Shionogi recalls

Shionogi has 5 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 24 Jan 2018. The most frequent reason is potency & assay.

Total recalls5since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 24 Jan 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 1 20%Class III 4 80%

Why shionogi is recalled

Potency & Assay480%
Particulate Matter120%

By year

2018120%
2017240%
2015120%
2012120%

All shionogi recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
24 Jan 2018Drug	CLASS III	Mefenamic Acid Capsules, USP, 250 mg recalled by Shionogi	Shionogi	Particulate Matter	Nationwide
26 Jul 2017Drug	CLASS III	Mefenamic Acid, 250mg capsules recalled by Shionogi	Shionogi	Potency & Assay	Nationwide
26 Jul 2017Drug	CLASS III	Ponstel (Mefanamic Acid) recalled by Shionogi	Shionogi	Potency & Assay	Nationwide
12 Aug 2015Drug	CLASS III	Nisoldipine Extended Release Tablets, 17 mg recalled by ShionogiNisoldipine	Shionogi	Potency & Assay	Nationwide
4 Jul 2012Drug	CLASS II	Nisoldipine Extended Release Tablets, 17mg recalled by Shionogi	Shionogi	Potency & Assay	PA

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.