Platinium Dfr Vr Icd, Dr Icd, And Sonr Crt-d (2018-03-16)
Recall Summary Platinum DFR VR ICD, DR ICD, and SonR CRT-D devices (implantable heart devices) are being recalled across Canada due to a medical device issue. This recall affects patients who have received these implantable cardioverter-defibrillators. The FDA classified this as a Class I recall, the most serious category.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-03-23
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/18a24399-712c-44a1-b5f8-d323d98b9d75