Radspeed Manual / Auto
- Recalling firm
- Shimadzu Medical Systems NZ Ltd
- Product
- Radspeed Manual / Auto. [Device]
- Reason
- The manufacturer has identified that the indication of the publication year of the standard on the laser classification label attached to the line marker option of the Collimator type R-20J was incorrect., It was mislabelled as year 2001 instead of year 2007
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-02-17
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/85ed27a0-e759-4164-aca2-b0d70835c676