FDA Device recall Z-0269-2020
VITROS chemistry Products K+ Slides, Catalog No. 8157596
- FDA Device
- Class II
- terminated
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of VITROS chemistry Products K+ Slides, Catalog No. 8157596 by Ortho Clinical Diagnostics, citing users may experience intermittent slide dispense issues with some cartridges due to the anti-backup platen failing to advance inside the cartridge.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0269-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-09-10 |
| Published | 2019-11-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ortho Clinical Diagnostics |
| Distribution | US |
Product
VITROS chemistry Products K+ Slides, Catalog No. 8157596. MicroSlides which contain reagents in a dry, multi-layered form.
Reason
Users may experience intermittent slide dispense issues with some cartridges due to the anti-backup platen failing to advance inside the cartridge.
Identifiers
| code_info | 410209876551 410209876548 410209876539 410209950186 410209950196 410209950232 410209960354 410209960373 4102099…410209876551 410209876548 410209876539 410209950186 410209950196 410209950232 410209960354 410209960373 410209960330 410209960477 410209960495 410209970685 410209970716 410209970763 410209960548 410209960590 410209960591 410209960625 410209960626 410209970818 410209971322 410209971446 410209971447 410209971483 410209971484 410209971485 410209971602 410209971699 410209981652 410209981767 410209991938 410209991939 410210003291 410210003396 410210003507 410210003510 410210023496 410210023498 410210003645 410210003669 410210003719 410210003775 410210013798 410210013912 410210013938 410210013966 410210013996 410210014061 410210014053 410210024095 410210014134 410210024167 410210024196 410210024284 410210024342 410210024403 410210024438 410210024469 410210024506 410210044598 410210054742 410210044699 410210044700 410210044751 410210044842 410210045037 410210045051 410210045095 410210045097 410210045186 410210055198 410210 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0269-2020%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.