PlainRecalls
FDA Devices Moderate Class II Terminated

CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189

Reported: September 11, 2019 Initiated: July 10, 2019 #Z-2473-2019

Product Description

CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189

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
200 units
Distribution
CA FL MO TX MN AL GA NC IL PA
Location
Allentown, PA

Frequently Asked Questions

What product was recalled?
CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189. Recalled by B. Braun Medical, Inc.. Units affected: 200 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-2473-2019.