Terumo Cardiovascular Procedure Kit- X-Coated Pump and Table Pack… — Class II medical device recall Z-1465-2014
Terminated recall by Terumo Cardiovascular Systems Corp, reported 2014-04-23, distributed in CA. Incorrect customer notification label applied to the Tyvek lid of this specific lot of Terumo¿ Cardiovascular
| Recall number | Z-1465-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Terumo Cardiovascular Systems Corp, Ashland, MA, United States |
| Recall initiated | 2014-03-28 |
| Classified | 2014-04-16 |
| Reported by FDA | 2014-04-23 |
| Terminated | 2014-12-12 |
| Distributed | CA |
| Quantity | 37 units |
| Reason classes | labeling |
| Lot numbers | RA-27 |
| Model numbers | 73431 |
Product
Terumo Cardiovascular Procedure Kit- X-Coated Pump and Table Pack with FX25RE Catalog Number: 73431
Reason for recall
Incorrect customer notification label applied to the Tyvek lid of this specific lot of Terumo¿ Cardiovascular Procedure Kits
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-1465-2014. 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.