Hospira recalls
Hospira has 225 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 31 May 2017. 10 are still ongoing. The most frequent reason is sterility.
Total recalls225since 2012
Last 12 months0reported
Class I6027% of total
Ongoing10latest 31 May 2017
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 60 27%Class II 153 68%Class III 12 5%
Why hospira is recalled
Product types
Brands
By year
Ongoing hospira recalls
10 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Infant 25% Dextrose Injection recalled by HospiraDextrose | Hospira | Particulate Matter | Nationwide |
| Drug | CLASS I | Magnesium Sulfate Inj., USP 50%/mL) recalled by Hospira | Hospira | Particulate Matter | Nationwide |
| Drug | CLASS I | 4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL) (84 mg/mL) recalled | Hospira | Particulate Matter | Nationwide |
| Drug | CLASS III | Magnesium Sulfate Inj., USP 50%/mL) recalled by Hospira | Hospira | Potency & Assay | Nationwide |
| Drug | CLASS III | Quelicin (Succinylcholine Chloride) Injection, USP 200 mg recalledQuelicin | Hospira | Foreign Material | Nationwide |
| Drug | CLASS III | Normosol-M and 5% Dextrose (multiple electrolytes recalled by Hospira | Hospira | Other | Nationwide |
All hospira recalls, newest first
225 totalAbout 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.