HOSPIRA Inc., LAKE FOREST Recalls

Overview of recall records associated with HOSPIRA Inc., LAKE FOREST, including dates, categories and classifications where available.

2recall records

Jun 13, 2018latest record date

Aug 16, 2017earliest record date

Recall history in this database

Classification mix: Class II: 1, Class I: 1.

DrugJun 13, 2018

Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use recall — FDA D-0906-2018

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

Class IFDA: TerminatedHOSPIRA Inc., LAKE FOREST

DrugAug 16, 2017

Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial. recall — FDA D-1082-2017

Presence of Particulate Matter: Silicone oil

Class IIFDA: TerminatedHOSPIRA Inc., LAKE FOREST

Understanding this recall history

This page summarizes recall records in which the official source identifies HOSPIRA Inc., LAKE FOREST as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.