HOSPIRA, INC.
⚠️ Moderate Risk
FEI: 3016589778 • New York, NY • UNITED STATES
FEI Number
3016589778
Location
New York, NY
Country
UNITED STATESAddress
235 E 42nd St, , New York, NY, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
AGR RX
The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/22/2023 | 62ODP13VERAPAMIL HYDROCHLORIDE (ANTI-HYPERTENSIVE - PART II) | 179AGR RX | Division of West Coast Imports (DWCI) |
| 3/22/2023 | 60TDP14NALOXONE HCL (ANTAGONIST) | 179AGR RX | Division of West Coast Imports (DWCI) |
| 3/22/2023 | 65HDK04HETASTARCH (PLASMA VOLUME EXTENDER) | 179AGR RX | Division of West Coast Imports (DWCI) |
| 3/22/2023 | 64GDY27DESOGESTREL/ETHINYL ESTRADIOL (ESTROGEN) | 179AGR RX | Division of West Coast Imports (DWCI) |
| 3/22/2023 | 56CDK70CEFTRIAXONE SODIUM (CEPHALOSPORINS) | 179AGR RX | Division of West Coast Imports (DWCI) |
| 3/22/2023 | 65RDK01CALCIUM CHLORIDE (REPLENISHER) | 179AGR RX | Division of West Coast Imports (DWCI) |
| 3/22/2023 | 61KDO05ATROPINE SULFATE (ANTI-CHOLINERGIC) | 179AGR RX | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is HOSPIRA, INC.'s FDA import refusal history?
HOSPIRA, INC. (FEI: 3016589778) has 7 FDA import refusal record(s) in our database, spanning from 3/22/2023 to 3/22/2023.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. HOSPIRA, INC.'s FEI number is 3016589778.
What types of violations has HOSPIRA, INC. received?
HOSPIRA, INC. has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about HOSPIRA, INC. come from?
All FDA import refusal data for HOSPIRA, INC. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.