Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120392 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Chromophare Surgical Light System , REF CH00000001 | 2 | 04/09/2024 |
FEI # 3002975342 Stryker Communications |
| Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 | 2 | 03/27/2026 |
FEI # 3002975342 Stryker Communications |
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