Recall Z-2468-2019— B. Braun Medical, Inc.
Class II · Terminated
Class II FDA medical device recall by B. Braun Medical, Inc., initiated 2019-07-10, terminated 2020-08-21. FDA's recall record names no specific 510(k) clearance for this event. Product: FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160. Reason: The filter capacity is not achieved due to damage of the filter membrane..
- Recalling firm
- B. Braun Medical, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-07-10
- Terminated
- 2020-08-21
- Firm location
- Allentown, PA, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.