Peter Lazic Gmbh
Peter Lazic Gmbh appears in FDA public data with 5 recalls, 2 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-1277-2024, Class II) was initiated on October 6, 2023. Its most recent 510(k) clearance was granted on April 12, 2019.
Summary
- Total Recalls
- 5
- 510(k) Clearances
- 2
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1277-2024 | Class II | D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action. | October 6, 2023 |
| Z-1278-2024 | Class II | D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action. | October 6, 2023 |
| Z-1279-2024 | Class II | D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action. | October 6, 2023 |
| Z-1287-2024 | Class II | L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile | July 14, 2023 |
| Z-1288-2024 | Class II | L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile | July 14, 2023 |