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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K192302
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Product Description
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Recall
Class
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FDA Recall
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MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr... 2 11/04/2025 FEI # 3030574705
Mozarc Medical US LLC
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr... 2 11/04/2025 FEI # 3030574705
Mozarc Medical US LLC
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Safety Componen... 2 11/04/2025 FEI # 3030574705
Mozarc Medical US LLC
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 ... 2 11/04/2025 FEI # 3030574705
Mozarc Medical US LLC
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 ... 2 11/04/2025 FEI # 3030574705
Mozarc Medical US LLC
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr... 2 11/04/2025 FEI # 3030574705
Mozarc Medical US LLC
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