Health product recall

ABL800 FLEX System - Instrument Configurations (2020-02-24)

Starting date:
February 24, 2020
Posting date:
March 6, 2020
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-72501

Last updated: 2020-03-10

Affected Products

ABL800 FLEX System - Instrument Configurations

Reason

Recall due to reader has misinterpreted the contents of a barcode for patient ID or accession number used for e.g. sampler identification.

Affected products

ABL800 FLEX System - Instrument Configurations

Lot or serial number

Not applicable.

Model or catalog number

393-800

Companies
Manufacturer

Radiometer Medical Aps

Akandevej 21

Bronshoj

2700

DENMARK