Angiotech (Manan Medical Products, Inc.)
Angiotech (Manan Medical Products, Inc.) appears in FDA public data with 7 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0820-2019, Class II) was initiated on December 18, 2018.
Summary
- Total Recalls
- 7
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0820-2019 | Class II | Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x 5 cm - Product Usage: Manual surgical | December 18, 2018 |
| Z-0818-2019 | Class II | Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x 5 cm- Product Usage: Manual surgical | December 18, 2018 |
| Z-0817-2019 | Class II | Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm 14MTWX x 12.5 c | December 18, 2018 |
| Z-0816-2019 | Class II | J Type Bone Marrow Needle 13ga x 6cm - Product Usage: Manual surgical instruments for Bone Marrow | December 18, 2018 |
| Z-0814-2019 | Class II | "J" Type Bone Marrow Needle 11ga x 10 cm - Product Usage: Manual surgical instruments for Bone Mar | December 18, 2018 |
| Z-0815-2019 | Class II | J Type Bone Marrow Needle 13ga x 10 cm- Product Usage: Manual surgical instruments for Bone Marrow | December 18, 2018 |
| Z-0819-2019 | Class II | Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm | December 18, 2018 |