Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K953162 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal c... | 1 | 02/18/2026 | Olympus Corporation of the Americas |
| Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of the abdomina... | 1 | 02/18/2026 | Olympus Corporation of the Americas |
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