Medical Device Recalls
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1 result found
Recall Number: Z-1290-2025 |
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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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| (1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM... | 2 | 03/05/2025 |
FEI # 3004135191 LUMENIS, LTD. |
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