Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Naloxone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST Due to Presence of Particulate Matter; Potential for particulate matter...

Date: June 4, 2018
Company: HOSPIRA INC, LAKE FOREST
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact HOSPIRA INC, LAKE FOREST directly.

Affected Products

Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use cartridge syringe, Single unit (NDC 0409-1782-03) and 10 count box (NDC 0409-1782-69), Rx Only, Hospira Inc., Lake Forest, IL

Quantity: 164,860 syringes

Why Was This Recalled?

Presence of Particulate Matter; Potential for particulate matter on the syringe plunger.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About HOSPIRA INC, LAKE FOREST

HOSPIRA INC, LAKE FOREST has 4 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report