Fresenius 2008T BlueStar Hemodialysis Machine Part Number… — Class II medical device recall Z-1749-2020
Ongoing recall by Fresenius Medical Care Holdings, Inc., reported 2020-04-29, distributed nationwide. A "Remove USB Device 2" false alarm may be displayed when no USB device or a non-powered USB device is connect
| Recall number | Z-1749-2020 |
|---|---|
| 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 | 2020-03-12 |
| Classified | 2020-04-20 |
| Reported by FDA | 2020-04-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 15,342 |
Product
Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description: 191124 2008T HD SYS. CDX BLUEST AR; 191126 2008T HD SYS. CDX W/BIBAG BLUEST AR; 191128 2008T HD SYS. W/O CDX BLUEST AR; 191130 2008T HD SYS. W/O CDX W/BIBAG BLUEST AR
Reason for recall
A "Remove USB Device 2" false alarm may be displayed when no USB device or a non-powered USB device is connected to the USB port on the rear of the machine
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-1749-2020. 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.