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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 29 Results
510(K) Number: K790062
 
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Product Description
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Recall
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FDA Recall
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Gravity and Infusion Pump Intravenous (IV) Sets using the Y-site Ultrasite Valve including: Horizon ... 2 06/12/2003 FEI # 2523676
Braun,B Medical Inc
ADDitIV Primary IV Set with Universal Spike, Backcheck Valve, two Injection Sites and Spin-Lock Conn... 2 06/05/2009 FEI # 2523676
B. Braun Medical, Inc.
Ultrasite ADDitIV Primary IV Set with Universal Spike, Backcheck Valve, two Ultrasite Injection Site... 2 06/05/2009 FEI # 2523676
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
B.BRAUN utilized in gravity IV administration sets and pump administration sets utilized with BBMI's... 2 11/26/2025 FEI # 2521402
B Braun Medical Inc
Caresite utilized in gravity IV administration sets and pump administration sets utilized with BBMI'... 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
IV Administration Set utilized in gravity IV administration sets and pump administration sets utiliz... 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
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