The Metrix Company: Device Recall
Recall #Z-0336-2025 · 10/09/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0336-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- The Metrix Company
- Status
- Ongoing
- Date Initiated
- 10/09/2024
- Location
- Dubuque, IA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2549 cases of 50 units
Reason for Recall
A limited number of IV bags have been found to leak during filling.
Product Description
SECURE 100 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed), REF 66041; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Distribution Pattern
Worldwide - US Nationwide distribution in the states of TX, IL, OH, PA, WA, MD, IL, UT, CA, MA, PA, MI, FL, PR, and the country of Canada.
Other Recalls by The Metrix Company
- Class II: Risk 10/09/2024
- Class II: Risk 10/09/2024
- Class II: Risk 10/09/2024
- Class II: Risk 10/09/2024
- Class II: Risk 10/09/2024
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.