Maquet Cardiopulmonary Gmbh
3
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-09-23 to 2026-09-23
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-09-23 | FDA Device | FDA Recall: Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS); | Maquet Cardiopulmonary Gmbh | Class II | N/A |
| 2026-09-23 | FDA Device | FDA Recall: Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS); | Maquet Cardiopulmonary Gmbh | Class II | N/A |
| 2026-09-23 | FDA Device | FDA Recall: Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS); | Maquet Cardiopulmonary Gmbh | Class II | N/A |