ICU
ICU appears in FDA public data with 9 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2679-2017, Class II) was initiated on February 1, 2013.
Summary
- Total Recalls
- 9
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2679-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2681-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2683-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2675-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2678-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2677-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2676-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2682-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |
| Z-2680-2017 | Class II | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of | February 1, 2013 |