International safety notice
K1021
New Zealand / Medsafe Recalls · NZL · Feb 26, 2016
Key facts
| Title | K1021 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Siemens Dimension Blood Urea Nitrogen (BUN) Flex Reagent Cartridge |
| Manufacturer | Siemens Healthcare Diagnostics (UK) Ltd |
| Models | K1021 |
| Event type | Recall |
| Action type | Recall |
| Date | Feb 26, 2016 |
| Regulator page | medsafe.govt.nz |
At a glance
- Yes Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1