RTLR190395: 2008K@HOME MACHINE — Class II medical device recall Z-2347-2024
Ongoing recall by Fresenius Medical Care Holdings, Inc., reported 2024-07-17, distributed nationwide. An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period
| Recall number | Z-2347-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fresenius Medical Care Holdings, Inc., Waltham, MA, United States |
| Recall initiated | 2024-06-03 |
| Classified | 2024-07-11 |
| Reported by FDA | 2024-07-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 6 units |
| UPC / GTIN / UDI-DI | 00840861100958 |
| Serial numbers | 5K0S-322B, 5K0S-U131, 6K0S-052M, 6K0S-058N, 6K0S-472G, 6K0S-514F |
| Model numbers | F40015481, RTLR190395 |
Product
RTLR190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Reason for recall
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
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-2347-2024. 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.