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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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(1) CareEvent, Model No. 866435
(2) CareEvent Upgrade, Model no. 866436
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2
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01/13/2024
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FEI # 3006648320 Philips North America
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(1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3...
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2
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04/21/2023
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FEI # 3008002452 Carefusion 2200 Inc
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(1) CentraLink Data Management System software version 16.0.2 Siemens Material Number (SMN): 1131324...
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2
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06/26/2020
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FEI # 2432235 Siemens Healthcare Diagnostics, Inc.
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(1) Central Venous Catheterization Kit, Part Number (PN): ASK-04300-PHP; (2) Single-Lumen Central Ve...
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2
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04/10/2018
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FEI # 3015859709 Arrow International Inc
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(1) Centurion Sterile CirClamp, Reorder #200CR;
(2) Centurion CirClamp with 1.1cm Bell and Insert, ...
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2
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10/18/2024
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FEI # 1417592 MEDLINE INDUSTRIES, LP - Northfield
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(1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellular...
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2
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08/08/2024
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FEI # 3001451326 Artivion, Inc
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(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, M...
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2
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08/24/2022
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FEI # 2126677 GE Healthcare, LLC
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(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186.
(2) Genesis II Non-Poro...
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2
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07/20/2022
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FEI # 1020279 Smith & Nephew, Inc.
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(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile;
(2) Gibeck Humid-Vent 2S Flex DC, Produc...
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2
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05/24/2022
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FEI # 3005747797 TELEFLEX MEDICAL INC
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(1) Ingenia Ambition X (Product Number 781356);
(2) Ingenia Ambition S (Product Number 781359)
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2
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01/11/2024
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FEI # 3006648320 Philips North America
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