Recall – Patient identification software misinterprets specific barcodes

Company: Radiometer Medical ApS
Date of Enforcement Report: 4/15/2020
Class II

PRODUCT

ABL800 FLEX, model number/UDI 393-800/0570

  • In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2, cK+, cNa+, cCa2+, cCl , cGlu, cLac, cCrea, ctBil, and co-oximetry parameters (ctHb, sO2, and the hemoglobin fractions FO2Hb, FCOHb, FMetHb, FHHb and FHbF).
  • In vitro testing of samples of expired air for the parameters pO2 and pCO2 In vitro testing of pleura samples for the pH parameter.0693938004 and 393-801/05700693938011.

Recall Number: Z-1684-2020

REASON

Analyzer’s barcode reader misinterprets the contents of barcode label used for entering patient ID or accession number. The issue is related to barcode types not using a check digit. This could result in patient mixup or loss of sample resulting in delayed medical treatment

RECALLING FIRM/MANUFACTURER

Radiometer Medical ApS on 3/10/2020. Voluntary:  Firm Initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE

3,656 units

DISTRIBUTION

US Nationwide and International

Upcoming Public Courses

No public courses are planned at this time.

If you would like to discuss a private, onsite course, please fill out the form below.

Or just email training@softwarecpr.com for more info.

Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.