FDA Device recall Z-1552-2015
2008 Series Hemodialysis Machines: 2008K2 with the following product code and description: 190633 2008K2 HEMO SYSTEM, OPTIONAL MODULE
- FDA Device
- Class II
- terminated
- Published 2015-05-06
On 2015-05-06 the FDA classified a Class II recall of 2008 Series Hemodialysis Machines: 2008K2 with the following product code and description: 190633 2008K2 HEMO SYSTEM, OPTIONAL MODULE by Fresenius Medical Care Holdings, citing the Acetate value for GranuFlo on the Select Concentrate screen should be 8mEq/l but it is displayed as 4mEq/l. The correct value is shown on the dialysate screen.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1552-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-02-20 |
| Published | 2015-05-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Fresenius Medical Care Holdings |
| Distribution | US |
Product
2008 Series Hemodialysis Machines: 2008K2 with the following product code and description: 190633 2008K2 HEMO SYSTEM, OPTIONAL MODULE; 190618 2008K2 HEMODIALYSIS SYS OLC/DP, SPANISH; 190610 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS; 190630 2008K2 MACHINE, SHORT CAB, OLC/DP, HP; 190628 2008K2 OLC ONLY WITH HEPARIN PUMP The Fresenius 2008K is indicated for acute and chronic dialysis therapy.
Reason
The Acetate value for GranuFlo on the Select Concentrate screen should be 8mEq/l but it is displayed as 4mEq/l. The correct value is shown on the dialysate screen.
Identifiers
| code_info | Serial Numbers: 0K0S-0678 0K0S-0885 0K0S-0901 0K0S-0917 0K0S-0922 0K0S-0927 0K0S-0935 0K0S-0943 0K0S-0959 0K0…Serial Numbers: 0K0S-0678 0K0S-0885 0K0S-0901 0K0S-0917 0K0S-0922 0K0S-0927 0K0S-0935 0K0S-0943 0K0S-0959 0K0S-0960 0K0S-0963 0K0S-0992 0K0S149209-149999 0K0S150000- 152000 0K0S152001- 154000 0K0S154001- 160000 0K0S160001- 162000 0K0S162001- 165353 0S154030 1K0S-1000 1K0S-1022 1K0S-1027 1K0S-1029 1K0S-1035 1K0S-1037 1K0S-1044- 1046 1K0S-1065 1K0S-1067 1K0S-1070 1K0S-1094 1K0S-1095 1K0S-1102 1K0S-1103 1K0S-1121 1K0S165354- 174103 2K0S174104 2K0S174105- 174111 2K0S174150- 182134 2K0S-5783 2K0S-5802 2K0S-6015 2K0S-6046 2K0S-6065 2K0S-6067 2K0S-6109 2K0S-6232 2K0S-6266 2K0S-9573 3K0S182135- 188639 4K0S188640- 192508 4K0S192542 4K0S192545 4K0S192550- 192553 4K0S192555 4K0S192566- 192569 4K0S192571 4K0S192572 4K0S192575- 192577 4K0S192579 4K0S192581 4K0S192584- 192586 4K0S192588 4K0S192593 4K0S192602 4K0S192603 4K0S192605 4K0S192675 4K0S192738- 192740 4K0S-N592 4K0S-Q302 4K0S-Q350 4K0S-Q362 4K0S-Q425 4K0S-Q467 4K0S-Q4 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1552-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.