Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1688-2016 - LenSx Laser System. Indicated for use in patients undergoing cataract surgery and refractive surgery. | 2 | 05/17/2016 | Alcon Research, Ltd. |
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