Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K183605 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cirq Arm System - Model SBS 1.3.2 (Art.No. 56000-01B) and SBS 1.4 (Art.No. 56000-01C) of the CIRQ Ar... | 2 | 08/29/2020 | Brainlab AG |
| BRAINLAB Curve; Model/catalogue (article) numbers for Curve: 19901; 19901B; 19900; 19905 UDI (GTIN... | 2 | 08/13/2020 | Brainlab AG |
| BRAINLAB Kick 2; Model/catalogue (article) numbers for Kick: 18170; 18070 UDI (GTIN) for Kick: 040... | 2 | 08/13/2020 | Brainlab AG |
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