Hospira Inc Lake Forest recalls
Hospira Inc Lake Forest has 4 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 13 Jun 2018. The most frequent reason is particulate matter.
Total recalls4since 2017
Last 12 months0reported
Class I125% of total
Ongoing0latest 13 Jun 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 25%Class II 3 75%Class III 0 0%
Why hospira inc lake forest is recalled
Product types
Brands
By year
All hospira inc lake forest recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Naloxone Hydrochloride Injection, USP, 0.4 mg/mL recalledNaloxone Hydrochloride | Hospira Inc Lake Forest | Particulate Matter | Nationwide |
| Drug | CLASS II | Hydromorphone Hydrochloride Injection, USP, 50 mg recalledHydromorphone Hydrochloride | Hospira Inc Lake Forest | Particulate Matter | Nationwide |
| Drug | CLASS II | Hydromorphone Hydrochloride Injection, USP, 500 mg recalledHydromorphone Hydrochloride | Hospira Inc Lake Forest | Particulate Matter | Nationwide |
| Drug | CLASS II | Hydromorphone Hydrochloride Injection, USP, 500 mg recalledHydromorphone Hydrochloride | Hospira Inc Lake Forest | Particulate Matter | 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.