NaturaLyte Liquid Acid Concentrate 2.0 mEq/L, Model # 08-2251-0 3.43 liter bottle This concentrate is formulated to be used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
FDA Recall Z-1010-2018 · Posted None
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Recalling FirmFresenius Medical Care Renal Therapies Group, LLC
Recall StatusTerminated
Product CodeKPO
Date Initiated2017-09-29
Date Terminated2018-08-09
Product Quantity598 cases
Reason for Recall
The label specifies the potassium concentration is 2.0 mEq/L. Some of the product in the affected lot was
found to have a potassium concentration of 2.25 mEq/L.
Firm Action
The firm, Fresenius Medical Care, sent an "URGENT - MEDICAL DEVICE RECALL" letter dated 10/4/2017 to its Consignees. The letter described the product, problem and actions to be taken. The Consignees are instructed to:
" Immediately examine your stock to determine whether you have any Naturalyte Liquid Acid Concentrate from the lot listed.
" If any product of this lot is found, discontinue use immediately.
" Place all units in a secure, segregated area.
" Contact your FMCRTG, LLC Customer Service Team at 1-800-323-5188 for instructions on how to return the recalled product.
" Promptly fill out and return the attached Reply Form via fax to: 781-699-9796 ATTN: Quality Department or SCAN and email to: [email protected].' and
"Route the letter to others in your organization that may have any of the affected product that is subject to this recall.
Please note that the Naturalyte Liquid Acid Concentrate matching the Lot Number listed in the notification is the only lot subject to this recall.
If you have any additional medical concerns or questions, please contact Medical Information and Communication: 855-616-2309 or Website: www.fresenius-medinfo.com.
Root Cause
Release of Material/Component prior to receiving test results
Distribution Pattern
US Distribution to states of: CA, FL, KS, LA, and TX.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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