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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K152208
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Recall
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Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile, single-use, disposable set u... 2 04/25/2025 FEI # 1219702
Belmont Instrument LLC
Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038. Sterile, single-use, disp... 2 04/25/2025 FEI # 1219702
Belmont Instrument LLC
Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile, single-use, disposa... 2 04/25/2025 FEI # 1219702
Belmont Instrument LLC
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