Z-2468-2019 Class II Terminated
FDA device recall Z-2468-2019 was initiated by B. Braun Medical, Inc. on July 10, 2019 and is designated Class II. Reason for recall: The filter capacity is not achieved due to damage of the filter membrane. The recall status is terminated (terminated August 21, 2020). Affected quantity: 250 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 11, 2019
- Initiation Date
- July 10, 2019
- Termination Date
- August 21, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 250 units
Product Description
FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160
Reason for Recall
The filter capacity is not achieved due to damage of the filter membrane.
Distribution Pattern
CA FL MO TX MN AL GA NC IL PA
Code Information
Lot # 0061526085 UDI: 04046964941054