Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K012842 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Adult Resuscitator, Pro-5000 Series, Single Patient Use, The Disposable Resuscitators with opti... | 1 | 11/01/2012 | Ventlab Corporation |
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