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
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0229-04 - ISPAN patient bracelet, given to patients post surgery to warn of further use of dinitrogen monoxide | 2 | 12/17/2003 |
FEI # 1610287 Alcon Laboratories, Inc |
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