FDA Device recall Z-2784-2015
Merlin@home RF Remote Monitoring Transmitter Model EX1150
- FDA Device
- Class II
- terminated
- Published 2015-09-23
On 2015-09-23 the FDA classified a Class II recall of Merlin@home RF Remote Monitoring Transmitter Model EX1150 by St Jude Medical Cardiac Rhythm Management Division, citing some devices exhibit backup VVI operation due to a backup reset.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2784-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-18 |
| Published | 2015-09-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | St Jude Medical Cardiac Rhythm Management Division |
| Distribution | US |
Product
Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid in the remote support of SJM implantable pacemakers and ICD's.
Reason
Some devices exhibit backup VVI operation due to a backup reset.
Identifiers
| code_info | Model: EX1150 Serial #: 02902036 05103228 12200027 12200047 12200063 12200065 12200071 12200093 12200100 122…Model: EX1150 Serial #: 02902036 05103228 12200027 12200047 12200063 12200065 12200071 12200093 12200100 12200111 12200120 12200122 12200157 12200165 12200168 12200174 12200187 12200235 12200245 12200250 12200331 12200333 12200351 12200367 12200369 12200371 12200399 12200432 12200449 12200459 12200466 12200471 12200478 12200522 12200539 12200574 12200582 12200621 12200641 12200658 12200661 12200679 12200680 12200700 12200738 12200749 12200754 12200758 12200771 12200772 12200788 12200791 12200800 12200832 12200845 12200850 12200851 12200864 12200868 12200877 12200891 12200892 12200906 12200914 12200945 12200963 12200965 12200966 12200967 12200972 12200975 12200976 12200977 12200978 12200980 12200987 12200991 12200992 12200997 12200999 12201000 12201001 12201002 12201005 12201006 12201007 12201008 12201010 12201011 12201016 12201019 12201020 12201025 12201026 12201036 12201037 12201038 1220 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2784-2015%22
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