Purewick Corporation
Purewick Corporation appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1485-2017, Class II) was initiated on February 24, 2016.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1485-2017 | Class II | PureWick External Catheter for Women-Wick Product Usage: A flexible, contoured external cathete | February 24, 2016 |