RMU-2000 Automated Chest Compression Device — Class I medical device recall Z-2543-2024
Ongoing recall by Defibtech, LLC, reported 2024-08-21, distributed in CT, FL, NJ, SC, TN. Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy i
| Recall number | Z-2543-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Defibtech, LLC, Guilford, CT, United States |
| Recall initiated | 2024-07-12 |
| Classified | 2024-08-14 |
| Reported by FDA | 2024-08-21 |
| Distributed | CT, FL, NJ, SC, TN |
| Countries outside the US | JP |
| UPC / GTIN / UDI-DI | 00815098020812, 10815098020819 |
| Serial numbers | 502000064, 502000067, 502000068, 502000072, 502000074, 502000078, 502000201, 502000202, 502000203, 502000204, 502000205, 502000206, 502000207, 502000209, 502000210, 502000211, 502000212, 502000213, 502000215, 502000216, 502000217, 502000218, 502000219, 502000220, 502000221 and 191 more |
Product
RMU-2000 Automated Chest Compression Device
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2543-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.