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
Reported: June 13, 2018 Initiated: June 4, 2018 #D-0906-2018
Product Description
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
Reason for Recall
Presence of Particulate Matter; Potential for particulate matter on the syringe plunger.
Details
- Recalling Firm
- HOSPIRA INC, LAKE FOREST
- Units Affected
- 164,860 syringes
- Distribution
- Nationwide in the U.S., Puerto Rico, and Guam
- Location
- LAKE FOREST, IL
Frequently Asked Questions
What product 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. Recalled by HOSPIRA INC, LAKE FOREST. Units affected: 164,860 syringes.
Why was this product recalled? ▼
Presence of Particulate Matter; Potential for particulate matter on the syringe plunger.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 13, 2018. Severity: Critical. Recall number: D-0906-2018.
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