International safety notice
HEP0001|HEP0001-AU|HEP0001-BR|HEP0001-CN|HEP0001-JP|HEP0001-UK|HEP0001-US|HEP1001|HEP1001-AU|HEP1001-US|HEP1001CON4869|HMX1350-1
New Zealand / Medsafe Recalls · NZL · Apr 11, 2022
Key facts
| Title | HEP0001|HEP0001-AU|HEP0001-BR|HEP0001-CN|HEP0001-JP|HEP0001-UK|HEP0001-US|HEP1001|HEP1001-AU|HEP1001-US|HEP1001CON4869|HMX1350-1 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Sara 3000, Plus, Lite, Flex, Combilizer. Maxi Twin, Compact, Move, 500. Maxi Sky 440, 600, 1000, Maxi Sky 2, Maxi Sky 2 Plus, Maxi Lite, Walker, Minstrel, Tenor; Miranti; Voyager; Bolero |
| Manufacturer | ArjoHuntleigh AB |
| Models | HEP0001-US, HEP0001-AU, HEP0001, HEP1001-US, HEP1001, HEP1001-AU, HEP0001-JP, HMX1350-1, HEP0001-CN, HEP1001CON4869, HEP0001-UK, HEP0001-BR |
| Event type | Safety Notice |
| Action type | Correction |
| Date | Apr 11, 2022 |
| Regulator page | medsafe.govt.nz |
At a glance
- No Recall
- Yes Field safety notice
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