D-1270-2020 Class I Terminated
FDA drug recall D-1270-2020 was initiated by ICU Medical Inc on May 8, 2020 and is designated Class I. Reason for recall: Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide. The recall status is terminated (terminated November 10, 2021). Affected quantity: 93,648 flexible container.
Recall Details
- Product Type
- Drugs
- Report Date
- May 27, 2020
- Initiation Date
- May 8, 2020
- Termination Date
- November 10, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 93,648 flexible container
Product Description
LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Reason for Recall
Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
Distribution Pattern
Nationwide within the United States
Code Information
Lot #: 07-514-FW Exp. 01-JUL-2021