Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K192143 |
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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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| Volara System. Blue Ventilator Adapter Module. Intermittent positive pressure breathing device comp... | 1 | 07/17/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
| Volara System. Single Patient Use (SPU) Circuit 5kit for Volara and Single Patient Use (SPU) Circuit... | 1 | 07/17/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
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