Heparin Sodium recalls

Heparin Sodium products have been recalled 5 times, most recently on 15 Mar 2023. The recalling company is usually Hospira. The most common reason is sterility.

Total recalls5since 2014

Last 12 months0reported

Class I120% of total

Ongoing0latest 15 Mar 2023

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

Why heparin sodium is recalled

Companies

Product types

Blood Thinners5100%

By year

2023240%
2014360%

All heparin sodium recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
15 Mar 2023Drug	CLASS II	Heparin Sodium Injection, USP, 20,000 USP units per mL recalledHeparin Sodium	Sagent Pharmaceuticals	Other	Nationwide
11 Jan 2023Drug	CLASS II	Heparin Sodium 2,000, USP Units, per (2 USP Units/mL) recalled by PfizerHeparin Sodium	Pfizer	Sterility	Nationwide
31 Dec 2014Drug	CLASS I	Heparin Sodium, 1000 USP Heparin Units recalled by HospiraHeparin Sodium	Hospira	Particulate Matter	Nationwide
12 Mar 2014Drug	CLASS II	Heparin Sodium Injection, USP 10,000 USP units recalledHeparin Sodium	Fresenius Kabi USA	Potency & Assay	Nationwide
5 Feb 2014Drug	CLASS II	Heparin Sodium 2000 USP Heparin Units recalled by HospiraHeparin Sodium	Hospira	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.