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Recall Observatory FDA recall evidence

Device product

ENVOY 500 ISE CALIBRATOR KIT, reference 55117 (contained 6 x 20 mL Calibrator High level and 6 x 20 mL Calibrator Low level). Model/Catalog Number: 55117

Z-2591-2018

April 18, 2017

Class II

Product summary

Firm
ELITech Clinical Systems SAS
Event
Event 80321
Status
Terminated
Classification
Class II
Quantity
N/A
Official record key
device-enforcement:Z-2591-2018

Official wording

Reason: ELITech Clinical Systems SAS initiated this recall because some users of ENVOY 500 ISE CALIBRATOR Kit (Part number: 55117), for Envoy 500 systems are observing trouble while calibrating with some vials. Users contacted the firm when they received the messages "ISE OUT OF REPRODUCIBILITY" or "ISE SLOPE OUT OF RANGE" (i.e., failed calibration). This has resulted in delay in obtaining patient results until the calibrator lot is replaced.

Code information: Lot number 7038 , Manufacture date 03/2017, Expiration date 02/2019

Distribution pattern: U.S. only. No gov. accounts. No international.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    ELITech Clinical Systems SAS initiated this recall because some users of ENVOY 500 ISE CALIBRATOR Kit (Part number: 55117), for Envoy 500 systems are observing trouble while calibrating with some vials. Users contacted the firm when they received the messages "ISE OUT OF REPRODUCIBILITY" or "ISE SLOPE OUT OF RANGE" (i.e., failed calibration). This has resulted in delay in obtaining patient results until the calibrator lot is replaced.