Naloxone Hydrochloride Injection recall: Particulate Matter
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…
Why was Naloxone Hydrochloride Injection recalled?
Presence of Particulate Matter; Potential for particulate matter on the syringe plunger.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
72680LL, Exp. 1DEC2018 (NDC 0409-1782-03); 76510LL, Exp. 1APR2019 (NDC 0409-1782-69)
- Product
- 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…
- Recalling firm
- HOSPIRA INC, LAKE FOREST
- Quantity
- 164,860 syringes
- Distribution
- Nationwide in the U.S., Puerto Rico, and Guam
- Recall date
- June 13, 2018
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)