CentriMag Acute Circulatory Support System Motor — Class I medical device recall Z-0221-2020
Terminated recall by Thoratec Switzerland GMBH, reported 2019-11-06, distributed nationwide. Reports have been received of the CentriMag Systems experiencing motor and pump issues resulting from electrom
| Recall number | Z-0221-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Thoratec Switzerland GMBH, Zurich, Switzerland |
| Recall initiated | 2019-08-22 |
| Classified | 2019-10-30 |
| Reported by FDA | 2019-11-06 |
| Terminated | 2024-04-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, CH, CL, CO, CR, DK, DO, ES, FI, FR, GB, HK, IL, IN, IT, MX, NL, PT, QA, RO, SE, SG, SI, TH, TW |
| UPC / GTIN / UDI-DI | 07640135140078 |
| Model numbers | 102956, 201-10002 |
Product
CentriMag Acute Circulatory Support System Motor, U.S. Model 102956 and OUS Model 201-10002, a component of the CentriMag Extracorporeal Blood Pumping System.
Reason for recall
Reports have been received of the CentriMag Systems experiencing motor and pump issues resulting from electromagnetic interference (EMI).
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-0221-2020. 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.