Zoll Medical X Series — Class II medical device recall Z-1311-2014
Terminated recall by ZOLL Medical Corporation, reported 2014-04-09, distributed nationwide. Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
| Recall number | Z-1311-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ZOLL Medical Corporation, Chelmsford, MA, United States |
| Recall initiated | 2014-03-05 |
| Classified | 2014-03-31 |
| Reported by FDA | 2014-04-09 |
| Terminated | 2021-01-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, CA, CL, CN, CZ, DK, FR, GB, HR, HU, IL, IT, JP, KR, KW, RU, SA, SG, TH, TR, ZA |
| Quantity | 3,169 units |
Product
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
Reason for recall
Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
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-1311-2014. 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.