Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-3144-2026 - Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS); | 2 | 09/11/2026 |
FEI # 3009507273 Maquet Cardiopulmonary Gmbh |
| Z-3146-2026 - Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS); | 2 | 09/11/2026 |
FEI # 3009507273 Maquet Cardiopulmonary Gmbh |
| Z-3145-2026 - Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS); | 2 | 09/11/2026 |
FEI # 3009507273 Maquet Cardiopulmonary Gmbh |
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