Recall Z-1384-2017— Beckman Coulter Inc.

Class II · Terminated

Class II FDA medical device recall by Beckman Coulter Inc., initiated 2017-01-30, terminated 2017-08-19. It names one FDA 510(k) clearance: K101852. Product: iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103, 800-7106, 800-7162, 800-7163, 800-7166, 800-3061. The iChem Velocity automated urine chemistry system is used to test for the following analytes in urine: ketones, blood, protein, glucose, bilirubin, urobilinogen, nitrite, leukocyte esterase, specific gravity, pH, ascorbic acid, color, and clarity. The iChem Velocity automated urine chemistry analyzer is intended to be used for in vitro measurement of various analytes in urine; it is intended for use only with the iChem Velocity urine chemistry strips. Reason: The probe misalignment or bending has the potential to lead to delay in reporting results or incorrect patient results..

Recalling firm
Beckman Coulter Inc.
Classification
Class II
Status
Terminated
Initiated
2017-01-30
Terminated
2017-08-19
Firm location
Brea, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103, 800-7106, 800-7162, 800-7163, 800-7166, 800-3061. The iChem Velocity automated urine chemistry system is used to test for the following analytes in urine: ketones, blood, protein, glucose, bilirubin, urobilinogen, nitrite, leukocyte esterase, specific gravity, pH, ascorbic acid, color, and clarity. The iChem Velocity automated urine chemistry analyzer is intended to be used for in vitro measurement of various analytes in urine; it is intended for use only with the iChem Velocity urine chemistry strips

Reason for recall

The probe misalignment or bending has the potential to lead to delay in reporting results or incorrect patient results.

Data sourced from openFDA. This site is unofficial and independent of the FDA.