Heparin Sodium recalls

Heparin Sodium products have been recalled 6 times, most recently on 28 Oct 2026. The recalling company is usually Hospira. The most common reason is sterility.

Total recalls6since 2014

Last 12 months1reported

Class I117% of total

Ongoing1latest 28 Oct 2026

Recalls per month, last 24 months

click a bar for that month

0Dec '24 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0 0Dec 0 0 0Mar 0 0 0Jun 0 0 0Sep 1 0

Severity split

Class I 1 17%Class II 5 83%Class III 0 0%

Why heparin sodium is recalled

Companies

Product types

Blood Thinners6100%

By year

2026117%
2023233%
2014350%

Ongoing heparin sodium recalls

1 active

Reported	Class	Recall	Company	Reason	Where
28 Oct 2026Drug	CLASS II	Heparin Sodium Injection recalled by Shenzhen TechdowHeparin Sodium	Shenzhen Techdow Pharmaceutical	Sterility	Nationwide

All heparin sodium recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
28 Oct 2026Drug	CLASS II	Heparin Sodium Injection recalled by Shenzhen TechdowHeparin Sodium	Shenzhen Techdow Pharmaceutical	Sterility	Nationwide
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.