International safety notice
722001|722002|722003|722005|722006|722008|722010|722011|722012|722013|722015|722019|722020|722022|722023|722025|722026|722027|722028|722029|722031|722033|722034|722035|722038|722039|722058|722400
New Zealand / Medsafe Recalls · NZL · Nov 24, 2015
Key facts
| Title | 722001|722002|722003|722005|722006|722008|722010|722011|722012|722013|722015|722019|722020|722022|722023|722025|722026|722027|722028|722029|722031|722033|722034|722035|722038|722039|722058|722400 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Philips Allura Xper and AlluraClarity X-ray systems |
| Manufacturer | Philips Medical Systems Nederland BV |
| Models | 722031, 722029, 722002, 722020, 722028, 722013, 722003, 722005, 722025, 722001, 722034, 722033 and 16 more |
| Event type | Safety Notice |
| Action type | Correction |
| Date | Nov 24, 2015 |
| Regulator page | medsafe.govt.nz |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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