FDA Device recall Z-0267-2020
VITROS chemistry Products Cl- Slides, Catalog No. 6844471 (which supports Urine CL-). MicroSlides which contain reagents in a dry, multi-la…
- FDA Device
- Class II
- terminated
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of VITROS chemistry Products Cl- Slides, Catalog No. 6844471 (which supports Urine CL-). MicroSlides which contain reagents in a dry, multi-la… 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-0267-2020 |
| 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 Cl- Slides, Catalog No. 6844471 (which supports Urine CL-). 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 | 401006613389 401006613500 401006613501 401006613608 401006613609 401006613648 401006613671 401006613712 4010066…401006613389 401006613500 401006613501 401006613608 401006613609 401006613648 401006613671 401006613712 401006613796 401006613843 401006613890 401006584017 401006614028 401006584103 401006584161 401006584214 401006584259 401006584230 401006644380 401006644436 401006644502 401006644529 401006644574 401006584374 401006644604 401006644649 401006644670 401006644705 401006644745 401006644800 401006644871 401006644893 401006644896 401006664973 401006665040 401006665041 401006665223 401006665225 401006665226 401006665248 401006665295 401006665227 401006665228 401006665229 401006665306 401006675376 401006675473 401006675474 401006675513 401006675514 401006675559 401006675477 401006675478 401006675501 401006675552 401006675553 401006675630 401006675631 401006675659 401006675660 401006675803 401006695852 401006695862 401006695908 401006695916 401006675801 401006675802 401006695945 401006676062 401006676063 401006696041 401006 |
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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-0267-2020%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.