Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K123196 |
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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| Palindrome Precision HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemod... | 1 | 07/07/2022 |
FEI # 1282497 Covidien Llc |
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