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U.S. Department of Health and Human Services

Class 2 Device Recall Diacap(R) Ultra Dialysis Fluid Filter

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 Class 2 Device Recall Diacap(R) Ultra Dialysis Fluid Filtersee related information
Date Initiated by FirmMarch 01, 2013
Date PostedApril 26, 2013
Recall Status1 Terminated 3 on September 03, 2014
Recall NumberZ-1183-2013
Recall Event ID 64504
510(K)NumberK052764 
Product Classification System, dialysate delivery, central multiple patient - Product Code FKQ
ProductDiacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis fluid.
Code Information Lot numbers 302950410, 309910111, 313050411, 314300511, 316040711, 316450711, 305880812, 306301012, and 306311012.  This recall was expanded on/about June 18, 2013 to include additional lot #s 305010113 and 305000113.
FEI Number 2523676
Recalling Firm/
Manufacturer		 B. Braun Medical, Inc.
901 Marcon Boulevard
Allentown PA 18109-9512
For Additional Information ContactCustomer Support
800-848-2066
Manufacturer Reason
for Recall		There is the potential of the residual moisture of the Diacap Ultra membrane being reduced over time, which results in the reduction of the membrane permeability (ultrafiltration coefficient).
FDA Determined
Cause 2		Process design
ActionB. Braun Medical Inc. sent and "URGENT RECALL NOTICE" dated February 28, 2013 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. Contact the Customer Support Department at (800) 848-2066 for questions regarding this issue. This recall was expanded on/about June 18, 2013 to include additional lot #s 305010113 and 305000113. Customers were notified via certified mail on/about June 14, 2013.
Quantity in Commerce1580
DistributionDistribution and manufacturing dates for the expansion lots was reported as 5/23-6/14/2013 and 1/22-24/2013 respectively. Nationwide Distribution including the states of AZ, CA, DE, FL, GA, HI, IA, ID, IL, KS, KY, LA, MN, MO, NJ, NM, NY, OH, OR, PA, SC, SD, TN, TX, UT, WA and WV.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = FKQ
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