Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K810637 |
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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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| (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 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 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 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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