FEF 100n Flat Epidural Filter Nrfit recall
FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160
Why was FEF 100n Flat Epidural Filter Nrfit recalled?
The filter capacity is not achieved due to damage of the filter membrane.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # 0061526085 UDI: 04046964941054
- Product
- FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160
- Recalling firm
- B. Braun Medical, Inc.
- Quantity
- 250 units
- Distribution
- CA FL MO TX MN AL GA NC IL PA
- Recall date
- September 11, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)