FDA Device recall Z-2508-2020
Azure S DR MRI, Model Number W3DR01
- FDA Device
- Class II
- ongoing
- Published 2020-07-15
On 2020-07-15 the FDA classified a Class II recall of Azure S DR MRI, Model Number W3DR01 by Medtronic Cardiac Rhythm And Heart Failure Crhf, citing there is a rare communication sequence during the first device interrogation with a SmartSync Device Manager that may result in the temporary suspension of some device features (i….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2508-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-06-04 |
| Published | 2020-07-15 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medtronic Cardiac Rhythm And Heart Failure Crhf |
| Distribution | n/a |
Product
Azure S DR MRI, Model Number W3DR01
Reason
There is a rare communication sequence during the first device interrogation with a SmartSync Device Manager that may result in the temporary suspension of some device features (i.e., battery measurements, Capture Management", Atrial Lead Position Check", EffectivCRT" algorithms, and AdaptivCRT"). This rare interaction results in temporary suspension of automatic threshold testing and output adjustments, and suspension of auto-optimization of CRT therapy. The issue is unlikely to result in clinical impact to the patient, and features are restored upon next programmer device interrogation or presence of a magnet.
Identifiers
| code_info | serial numbers: RNJ200027H RNJ200025H RNJ200023H RNJ200022H RNJ200020H RNJ200018H RNJ200017H RNJ200015H RNJ200…serial numbers: RNJ200027H RNJ200025H RNJ200023H RNJ200022H RNJ200020H RNJ200018H RNJ200017H RNJ200015H RNJ200014H RNJ200011H RNJ200009H RNJ200008H RNJ200007H RNJ200006H RNJ200005H RNJ200004H RNJ200086H RNJ200085H RNJ200084H RNJ200083H RNJ200082H RNJ200081H RNJ200080H RNJ200078H RNJ200077H RNJ200076H RNJ200075H RNJ200074H RNJ200073H RNJ200072H RNJ200071H RNJ200070H RNJ200069H RNJ200068H RNJ200067H RNJ200066H RNJ200064H RNJ200063H RNJ200062H RNJ200061H RNJ200060H RNJ200059H RNJ200058H RNJ200057H RNJ200056H RNJ200055H RNJ200054H RNJ200052H RNJ200051H RNJ200050H RNJ200049H RNJ200048H RNJ200047H RNJ200046H RNJ200045H RNJ200043H RNJ200041H RNJ200040H RNJ200039H RNJ200038H RNJ200037H RNJ200036H RNJ200035H RNJ200034H RNJ200033H RNJ200032H RNJ200031H RNJ200030H RNJ200029H RNJ200028H RNJ200145H RNJ200144H RNJ200143H RNJ200142H RNJ200141H RNJ200140H RNJ200139H RNJ200138H RNJ200137H RNJ200135H RNJ200134H RNJ200133H |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2508-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.