Sekisui Diagnostics P.E.I recalls
Sekisui Diagnostics P.E.I has 2 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 1 Feb 2017. The most frequent reason is potency & assay.
Total recalls2since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 1 Feb 2017
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why sekisui diagnostics p.e.i is recalled
Product types
By year
All sekisui diagnostics p.e.i recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Sekisui Diagnostics Ammonia L3K¿ Assay recalled | Sekisui Diagnostics P.E.I | Potency & Assay | Nationwide |
| Device | CLASS II | Sekure Chemistry Sekisui Diagnostics Acetaminophen L3K recalled | Sekisui Diagnostics P.E.I | Potency & Assay | 10 states |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.