Medical Device Recalls
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1 result found
Recall Number: Z-0746-2016 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive h... | 2 | 02/03/2016 |
FEI # 1000115734 Resmed Corporation |
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