Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K780130 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BD ADD-ON Burette Set V/NV Needle-Free Valve, REF: 82113E-0006 | 2 | 09/13/2021 |
FEI # 3012410077 CAREFUSION |
| BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031... | 2 | 09/13/2021 |
FEI # 3012410077 CAREFUSION |
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