Recall Z-1098-2021

Roche Diagnostics Operations, Inc. · initiated January 6, 2021

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

9180 Electrolyte Analyzer - Product Usage: intended to be used for the measurement of sodium, potassium, chloride, ionized calcium and lithium in the whole blood, serum or plasma, urine, dialysate solutions, or QC materials. catalog number 03157334001 . in vitro diagnostic use.

Codes / lots: All Serial Numbers: U18.5093 U18.2418 U18.1099 U18.4188 U18.2819 13002 U18.3698 U18.4498 U18.3629 U18.3056 U18.3058 U18.2954 U18.4423 U18.4584 17769 U18.3657 U18.2026 U18.2245 13982 U18.2839 7148 7151 15061 27989 7143 U18.3533 U18.3590 U18.6311 U18.5772 5925 U18.5230 6265 U18.4798 U18.1900 17760 U18.3447 7157 U18.5809 U18.4696 U18.4698 19313 U18.3216 U18.3259 U18.3599 12853 U18.2144 U18.3519 U18.6131 U18.3648 U18.2430 U18.1138 U18.3137 U18.2334 U18.2972 U18.1554 U18.3537 U18.4440 U18.1160 U18.4014 U18.3324 U18.2006 24119 U18.3717 U18.1175 U18.1555 U18.4181 U18.2070 U18.6807 U18.2725 U18.1173 15217 U18.2172 U18.2727 U18.4357 U18.2441 15408 16650 22334 22336 U18.2277 U18.3052 U18.2110 U18.4254 U18.5501 U18.4755 U18.4230 U18.4365 U18.3638 U18.3089 15071 U18.3215 6836 6841 18016 U18.3789 U18.4243 U18.5644 U18.6395 U18.3390 U18.6644 U18.2679 U18.3096 U18.3064 U18.3635 12879 U18.3745 19537 17151 U18.4431 U18.3279 U18.4330 27753 19581 U18.2350 U18.4265 U18.1498 13667 U18.2828 U18.3384 25517 13983 13762 14981 15409 17202 14732 26969 U18.2946 U18.2789 U18.1461 U18.2593 U18.3397 U18.1772 U18.1777 U18.7156 U18.5830 U18.3613 12405 U18.4385 U18.3414 U18.1678 U18.5922 6981 U18.2814 U18.4750…

Reason for recall

May display Calcium results on the screen with wrong arrow direction which may lead to misinterpretation of results and incorrect medical decision. If the unit for iCa++ is set to mg/dL (configured as Service Code MGL) and a measured iCa++ value is lower than the normal range, an upward arrow is shown on the display instead of a downward arrow. The display is set per default to mmol/L; therefore, the arrow indicating an alarm reflects normal ranges of iCa++ in mmol/L. If mg/dL is chosen, the arrow warnings on screen still reflect the ranges from mmol/L, rather than mg/dL. The numeric result is displayed correctly.

FDA-determined cause: Software design

Action taken

Roche issued Urgent Medical Correction Letter on 1/6/2021, Urgent Medical Device Correction TP-01190 and Distributor UMDC TP-01192 mailed via UPS Ground. For iCa++ results, rely on the numeric value and units on the printout, rather than the analyzer display. Investigate where a change in result reporting could impact patient management. Consult with the physician, pathologist, or Laboratory Director at your facility to determine specific clinical implications for your patients. **** UPDATE 2/7/22: Customer Bulletin TP-01454 Customer Bulletin-Roche 9180 Electrolyte Analyzer Discontinuation of ISE Calcium Electrode. Customer Bulletins (TP-01454 and TP-01455) informing customers about discontinuation of distribution of the iCa electrode in the US mailed on 2/7/2022. Roche has decided to discontinue sales and distribution of the ISE Calcium Electrode (catalog number 03110354180) from the U.S. market by 4/30/2022. Until the calcium electrode is discontinued, use the workaround in UMDC TP-01190 pg 4, to report Ionized Calcium (iCa++) results: Make sure that iCa++ values are reported in mmol/L instead of mg/dL or contact your Roche Services representative. The guiding arrow on the display can be wrong if the unit for iCa++ is set to mg/dL (Service Code MGL configured) and if a measured iCa++ value is lower than the normal range. If you use the unit mg/dL for iCa++, always use arrow information from the printout and not from the display. After the calcium electrode is no longer available, refer to the Roche 9180 Electrolyte Analyzer IFU for proper installation of electrodes, including the use of a dummy electrode, when not all ISE tests are required. This document is available on eLabDoc at the dialog.roche.com website. Please contact the Roche Support Network Customer Support Center at 1-800-526-2272 if you have questions.

Details

Recall number
Z-1098-2021
Initiated
January 6, 2021
Posted by FDA
February 8, 2021
Terminated
February 28, 2024
Product code
JFP – Electrode, Ion Specific, Calcium
Quantity
1,214 units
Distribution
US Nationwide distribution.
Recalling firm
Roche Diagnostics Operations, Inc., Indianapolis, IN

Official FDA recall record