US Drug Recall Register
Class I · High risk Terminated Initiated Jun 4, 2018 (8 years ago)

Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

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

Recalling firm
Hospira INC, Lake Forest
NDC code
0409-1782-03
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0906-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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