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U.S. Department of Health and Human Services

Medical Device Recalls

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391 to 400 of 500 Results *
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Product Description
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Class
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FDA Recall
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(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model... 2 01/13/2024 FEI # 3006648320
Philips North America
(1) Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Featu... 2 04/10/2018 FEI # 3015859709
Arrow International Inc
(1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3)... 2 02/07/2025 FEI # 2016493
CareFusion 303, Inc.
(1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar Cup, E1 Antioxidant Infu... 2 10/09/2020 FEI # 1825034
Biomet, Inc.
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; ... 2 03/20/2018 FEI # 1818910
DePuy Orthopaedics, Inc.
(1) Teleflex Flex tube, Product #20011, sterile; (2) Teleflex Smooth-Flo Flex with Double Swivel, P... 2 05/24/2022 FEI # 3005747797
TELEFLEX MEDICAL INC
(1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement pro... 2 01/30/2023 FEI # 1825034
Biomet, Inc.
(1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement pros... 2 01/30/2023 FEI # 1825034
Biomet, Inc.
(1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-... 2 01/24/2020 FEI # 3012037425
Vitreq Bv
(1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ 23G BF Brush Needles-BF23... 2 01/24/2020 FEI # 3012037425
Vitreq Bv

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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