Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21116 |
| Brand Name: | ADVIA Chemistry Lactate Dehydrogenase (LDLP and LDPL) |
| Model: | |
| Affected: | ADVIA Chemistry Lactate Dehydrogenase L-P material numbers 10309501 (40mL) & 10341128 (70 mL), ADVIA Chemistry Lactate Dehydrogenase P-L material numbers 10309502 (40 mL) & 10341129 (70 mL) |
| Software version: | |
| Recalling Organisation: | Siemens Healthcare (NZ) Ltd Millennium Centre, Part Level 2, Building A 600 Great South Road Ellerslie AUCKLAND 1051 |
| Contact Information: | 0800 310 300 |
| Manufacturer: | Siemens Healthcare Diagnostics Inc |
| Issue: | The manufacturer is providing an update to all ADVIA Chemistry Systems Lactate Dehydrogenase L-P (LDLP) and Lactate Dehydrogenase P-L (LDPL) assay Instructions For Use (IFUs). The current ADVIA Chemistry Systems Lactate Dehydrogenase IFUs intended use section contains statements which will be removed: |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/2/2017 |
