Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K962826 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medline procedure kits labeled as: 1) A & A KNEE PACK-LF, Pack Number DYNJHS0136D; 2) ABD CLOSURE... | 2 | 03/25/2025 |
FEI # 1417592 MEDLINE INDUSTRIES, LP - Northfield |
| Medline Convenience kits labeled as: 1) MINOR BASIC PACK-LF, Pack Number DYNJ0281516M; 2) MINOR... | 2 | 09/06/2024 |
FEI # 1417592 MEDLINE INDUSTRIES, LP - Northfield |
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