Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16936 |
| Brand Name: | McKesson Horizon Cardilogy Hemodynamics system |
| Model: | Models: PB1000 & PB2000 |
| Affected: | |
| Software version: | Versions 12.2 HF4 and earlier |
| Recalling Organisation: | Device Technologies New Zealand 47 Arrenway Drive Albany AUCKLAND 0632 |
| Contact Information: | 09 913 2000 |
| Manufacturer: | Medcon Ltd |
| Issue: | McKesson has identified that its communication to customers regarding the required maintenance tests was insufficient. While each unit has an attached sticker indicating the date of the next maintenance test the need for performing annual maintenance testing is not reiterated in 12.2 HF4 and earlier versions of the Horizon Cardiology Hemo user guides. If the parameter boxes are not calibrated, the Horizon Cardiology Hemo system may not function properly or potentially affect the accuracy of clinical parameters. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/7/2014 |
