ICU Medical Inc: Drug Recall

Recall #D-0313-2021 · 03/09/2021

Class II: Risk

Recall Details

Recall Number
D-0313-2021
Classification
Class II
Product Type
Drug
Recalling Firm
ICU Medical Inc
Status
Terminated
Date Initiated
03/09/2021
Location
Lake Forest, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
425,628 bottles

Reason for Recall

Presence of particulate matter.one confirmed customer report of particulate matter within two semi-rigid bottles identified prior to use

Product Description

0.9% SODIUM CHLORIDE Irrigation, USP 1000 mL Semi-Rigid Bottle, Rx only, Manufactured for ICU Medical, Inc., Lake Forest, Illinois, 60045 USA. NDC 0990-7138-09

Distribution Pattern

Distributed Nationwide in the USA to include Puerto Rico

Other Recalls by ICU Medical Inc

View all recalls by ICU Medical Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.