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
- Class II: Risk 12/19/2025
- Class II: Risk 12/19/2025
- Class II: Risk 12/19/2025
- Class II: Risk 12/15/2025
- Class II: Risk 12/15/2025
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.