PlainRecalls
FDA Devices Moderate Class II Terminated

ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114

Reported: September 11, 2019 Initiated: July 10, 2019 #Z-2466-2019

Product Description

ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114

Reason for Recall

The filter capacity is not achieved due to damage of the filter membrane.

Details

Recalling Firm
B. Braun Medical, Inc.
Units Affected
100 units
Distribution
CA FL MO TX MN AL GA NC IL PA
Location
Allentown, PA

Frequently Asked Questions

What product was recalled?
ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114. Recalled by B. Braun Medical, Inc.. Units affected: 100 units.
Why was this product recalled?
The filter capacity is not achieved due to damage of the filter membrane.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 11, 2019. Severity: Moderate. Recall number: Z-2466-2019.