Cn - Synchromed Clinician Application A810
Recall Summary Medtronic Inc. is recalling the SynchroMed Clinician Application A810 software used in hospitals, pharmacies, and laboratories in New Zealand. The manufacturer is issuing guidance on how to use this product. This is classified as a Class I recall, the most serious type.
- Recalling firm
- Medtronic New Zealand Limited
- Product
- CN - SynchroMed Clinician Application A810. [Device]. Model: Multiple GTIN numbers
- Reason
- The manufacturerhas identified a software problem related to the Flex Infusion Mode in the SynchroMed A810 Clinician Programmer (CP) Software application (app) version 1.x and 2.x, used for the Model 8637 SynchroMed II and Model 8667 SynchroMed III Infusion pumps., When using the A810 Clinician Programmer app in Flex Infusion Mode, infusion steps should automatically display in chronological order. In rare cases, steps may appear out of order, preventing the Flex Infusion schedule from being delivered as intended or at all. Although the base rate continues to deliver correctly, missed flex...
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-04-07
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/850e4d64-d1b1-4161-a640-212b870ac60f