Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K974300 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Grasper/Retriever, Alligator Jaw, Rat Tooth 2.4 mm x 8 mm x 230 cm Catalog Number: 7226 Int... | 2 | 08/06/2021 | Shent USA, Inc. |
| Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208 Intended use: singl... | 2 | 08/06/2021 | Shent USA, Inc. |
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