Diazepam recalls

Diazepam products have been recalled 7 times, most recently on 15 Aug 2018. The recalling company is usually Hospira. The most common reason is sterility.

Total recalls7since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 15 Aug 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 6 86%Class III 1 14%

Why diazepam is recalled

Companies

Product types

Anxiety & Sleep Medication7100%

By year

2018114%
2016114%
2013457%
2012114%

All diazepam recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
15 Aug 2018Drug	CLASS III	Diazepam Rectal Gel, 5 mg, Twin Pack that Contains recalledDiazepam	Valeant Pharmaceuticals North America	Other	Nationwide
20 Jul 2016Drug	CLASS II	Diazepam Injection USP 10mg/ (5 mg/mL recalled by HospiraDiazepam	Hospira	Particulate Matter	Nationwide
4 Sep 2013Drug	CLASS II	Diazepam Injection, USP, 5 mg/mL recalled by HospiraDiazepam	Hospira	Sterility	Nationwide
12 Jun 2013Drug	CLASS II	Diazepam Injection, USP 5 mg/mL, Multiple-dose fliptop vial recalledDiazepam	Hospira	Sterility	Nationwide
15 May 2013Drug	CLASS II	Diazepam Injection, USP 5 mg/mL, Multiple-dose fliptop vial recalledDiazepam	Hospira	Sterility	Nationwide
8 May 2013Drug	CLASS II	Diazepam Injection, USP 5 mg/mL, Multiple-dose fliptop vial recalledDiazepam	Hospira	Sterility	Nationwide
20 Jun 2012Drug	CLASS II	Diazepam Injection, USP, 10 mg Automatic, Autoinjector recalledDiazepam	Meridian Medical Technologies a Pfizer	Potency & Assay	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.