Medical Device Recalls
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1 result found
Recall Number: Z-1332-2024 |
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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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| Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm) | 2 | 03/21/2024 |
FEI # 3002806863 D.O.R.C. Dutch Opthalmic Research Center Intl B.V. |
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