FDA Recall Terminated

DriSate Product Code DR-145 The acid concentrate powders and liquids are indicated for use in acute and chronic hemodialysis and to be used with the appropriate hemodialysis machine/monitor and bicarbonate concentrate.

Recall: Z-1869-2018 · Initiated April 7, 2018

Recall

Recall Number
Z-1869-2018
Event Number
79878
Firm
Rockwell Medical, Inc
FEI Number
3001236991
Product Code
KPO
Status
Terminated
Root Cause
Employee error
Initiated
April 7, 2018
Terminated
October 1, 2018
Address
30142 S. Wixom Rd., Wixom, MI, 48393-3440

Description

DriSate Product Code DR-145 The acid concentrate powders and liquids are indicated for use in acute and chronic hemodialysis and to be used with the appropriate hemodialysis machine/monitor and bicarbonate concentrate.

Reason

A subassembly component (dextrose bag) within this case product contained small amounts of sodium bicarbonate from a prior batch.

Action

Removal notification involved one customer and two facilities. The two facilities receiving the DR-145 kit lot were contacted directly via phone, email, and issuance of a RGA to return the product. Stock retrieval was completed by 4/7/17. See attached email and RGA. Communication was already completed and stock was retrieved. Discard and/or return via RGA provided The complaint documented a stock reconciliation in the complaint and all units were accounted for. The two customer facilities involved responded directly Affected kits were reworked to remove and replace the nonconforming dextrose bag. For further questions, please call (864) 849-0530.

Distribution

US Distribution to the state of NY

Quantity

139