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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K810637
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Product Description
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FDA Recall
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(1) Argon Medical Devices Double Female LL Adapter, Special Adapter to Convert a Male Fitting to Fem... 2 11/05/2019 FEI # 1625425
Argon Medical Devices, Inc
Argon Medical Devices Double Male LL Adapter, REF 040184800A, bulk, non-sterile. The firm name on t... 2 11/05/2019 FEI # 1625425
Argon Medical Devices, Inc
Argon Medical Devices AHD Luer Lock Cap, REF 501303, Sterile, Rx. The firm name on the label is Arg... 2 11/05/2019 FEI # 1625425
Argon Medical Devices, Inc
Argon Medical Devices Plugs, Male/Female Luer Lock Plug, REF 041295000A, 50/box, Sterile, Rx. The f... 2 11/05/2019 FEI # 1625425
Argon Medical Devices, Inc
Argon Medical Devices TRI-JECT, 3 Way IV Administration Organizer without Stopcock, REF 041230001A, ... 2 11/05/2019 FEI # 1625425
Argon Medical Devices, Inc
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