Cadence recalls
Cadence has 2 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 19 Aug 2015. The most frequent reason is foreign material.
Total recalls2since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 19 Aug 2015
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 cadence is recalled
Product types
By year
All cadence recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Perfectum Tuberculin Glass Syringe, Non sterile recalled by Cadence | Cadence | Foreign Material | Nationwide |
| Device | CLASS II | Micro-Mate Tuberculin Glass Syringe, Non-sterile recalled by Cadence | Cadence | Foreign Material | Nationwide |
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.