Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K803086 |
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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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| A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire Looped Electrode (M-21 SERIES... | 2 | 07/29/2019 |
FEI # 2242056 Alto Development Corp |
| Medline Convenience kits labeled as: CARDIAC PACING PACK, Pack Number DYNJ41223 | 2 | 09/06/2024 |
FEI # 1417592 MEDLINE INDUSTRIES, LP - Northfield |
| Medline Convenience kits labeled as: 1) CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036O; 2) CA... | 2 | 09/06/2024 |
FEI # 1417592 MEDLINE INDUSTRIES, LP - Northfield |
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