Medical Device Recalls
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1 result found
510(K) Number: K132553 |
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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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| CarePoint 60 mL Syringe Without Needle, REF: 04-7560 | 2 | 12/13/2022 |
FEI # 1000138447 Allison Medical, Inc. |
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