Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K153293 |
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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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| Anesthesia IV Set utilized in gravity IV administration sets and pump administration sets utilized w... | 2 | 11/26/2025 |
FEI # 2521402 B Braun Medical Inc |
| Anesthesia IV Set utilized in gravity IV administration sets and pump administration sets utilized w... | 2 | 11/26/2025 |
FEI # 2521402 B Braun Medical Inc |
| Extension Set utilized in gravity IV administration sets and pump administration sets utilized with ... | 2 | 11/26/2025 |
FEI # 2521402 B Braun Medical Inc |
| IV Administration Set utilized in gravity IV administration sets and pump administration sets utiliz... | 2 | 11/26/2025 |
FEI # 2521402 B Braun Medical Inc |
| Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034... | 2 | 04/29/2021 |
FEI # 2523676 B. Braun Medical, Inc. |
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