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-0546-06 - LIFEPAK 500 automated external defibrillator (AED) | 2 | 02/22/2006 |
FEI # 3015876 Medtronic Emergency Response Systems, Inc. |
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