Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Z-0274-2009 - PurePoint System Operator's Manual, Catalog Number 8065751131, Rev. B for use with the Alcon PurePoint Laser, Catalog Number 8065750597 Indicated for use in photocoagulation of both anterior and p... | 2 | 11/06/2008 | Alcon Laboratories, Inc. |
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