Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K153533 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Tearaway Introducer Set, REF: INT-028-27, INT-105-25, INT-106-09, INT-106-12, INT-106-17, DSS-007-04... | 2 | 06/15/2023 |
FEI # 3000718472 Galt Medical Corporation |
| Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16 | 2 | 06/15/2023 |
FEI # 3000718472 Galt Medical Corporation |
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