FDA Device recall Z-2543-2024
RMU-2000 Automated Chest Compression Device
- FDA Device
- Class I
- ongoing
- Published 2024-08-21
On 2024-08-21 the FDA classified a Class I recall of RMU-2000 Automated Chest Compression Device by Defibtech, citing problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or de….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2543-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-07-12 |
| Published | 2024-08-21 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Defibtech |
| Distribution | CT, FL, NJ, SC, TN |
Product
RMU-2000 Automated Chest Compression Device
Reason
Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or death.
Identifiers
| code_info | UDI-DI: 00815098020812, 10815098020819 Serial numbers 502001000 502000281 502000979 502000960 502000985 502000988 50200…UDI-DI: 00815098020812, 10815098020819 Serial numbers 502001000 502000281 502000979 502000960 502000985 502000988 502000264 502000201 502000973 502000249 502000248 502000205 502000216 502000217 502000275 502000204 502000234 502000267 502000270 502000237 502000232 502000227 502000907 502000908 502000980 502000987 502000078 502000074 502000064 502000072 502000224 502000235 502000223 502000225 502000231 502000222 502000245 502000246 502000932 502000220 502000938 502000934 502000945 502000946 502000922 502000958 502000927 502000944 502000942 502000236 502000943 502000941 502000238 502000998 502000250 502000948 502000068 502000294 502000939 502000284 502000212 502000247 502000067 502000966 502000963 502000929 502000903 502000953 502000272 502000937 502000296 502000226 502000260 502000262 502000211 502001050 502001006 502001055 502000935 502000952 502000240 502000206 502000263 502001054 502001073 502001047 502001067 502001008 502000996 502000265 502000969 502000968 502000933 502000279 502000 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2543-2024%22
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