Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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| Z-0802-2019 - ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800 | 2 | 02/05/2019 |
FEI # 3002655016 Arjohuntleigh Magog |
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