Cadence Inc.
Cadence Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2365-2015, Class II) was initiated on July 9, 2015.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2365-2015 | Class II | Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209 | July 9, 2015 |
| Z-2364-2015 | Class II | Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212 | July 9, 2015 |