Class II — Cadence Inc.
| Recalling firm | Cadence, Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel. |
| Product | Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212 |
| Quantity | 766 units |
| Distribution | Nationwide Foreign Canada, Denmark. Italy |
| Initiated | 2015-07-09 |
| Classified | 2015-08-10 |
| Terminated | 2016-07-29 |
| Recall number | Z-2364-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Cadence Inc. (Z-2364-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71674/
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