Product Wiki · Recalls · Health Canada — Medical Devices

RAPIDlab 1265 System - Analyzer (2015-05-06) — recall 53189

Health Canada — Medical Devices · Canada · 2015-06-01 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
53189
Date of alert
2015-06-01
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: During some internal testing at Siemens, it was discovered that the D50 (glucose sensor) and D51 (lactate sensor) error codes were not functioning on the RAPIDLab 1260 and RAPIDLab 1265 instruments. Glucose and lactate sensors that are not completely seated with the contacts on the instrument should alert the operator with a D50 (glucose sensor) error or a D51 (lactate sensor) error.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/rapidlab-1265-system-analyzer-

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