Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K172610 |
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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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| Olympus Thunderbeat, 5 mm, 35 cm, Front-Actuated Grip Type S | 2 | 02/17/2026 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S | 2 | 02/17/2026 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S | 2 | 02/17/2026 |
FEI # 2429304 Olympus Corporation of the Americas |
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