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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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TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visuali...
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3
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03/21/2022
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FEI # 3002646096 Cytocell Ltd.
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The Model 8540 Catheter Access Port Kit is intended for use in accessing the catheter via the cathe...
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2
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08/24/2004
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FEI # 2182207 Medtronic Inc, Neurological & Spinal Division
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The Thermedx Fluid Management System is designed to provide irrigation fluids to irrigate, distend,...
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2
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08/27/2014
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FEI # 3007495879 Thermedx LLC
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Thermo Scientific Microm: Rotary Microtome: REF HM355S-3
Used for slicing tissue blocks.
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2
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10/12/2011
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FEI # 1831638 Richard-Allan Scientific Company
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Titanium Trochanteric Fixation Nail (TFN)System
Intended to treat stable and unstable fractures ...
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2
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12/05/2013
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FEI # 3005180112 Synthes USA HQ, Inc.
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Triton Canister Software
Catalog Number: GAUS-2.
Intended adjunct in the estimation of blood lo...
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2
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02/27/2023
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FEI # 3015967359 Stryker Corporation
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Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features)
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2
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09/25/2010
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FEI # 3015859709 Arrow International Inc
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UROLOGY CUSTOMED PACK 5/CS
Used by medical staff to perform surgical procedures and patient car...
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2
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09/03/2015
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FEI # 2648727 Customed, Inc
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US Safire Duo Ablation Catheter MediGuide Enabled, REF A700240 and Cool Path Duo Ablation Catheter,...
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2
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11/06/2013
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FEI # 3005334138 St. Jude Medical
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VITALITY DR HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corporation...
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2
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07/11/2007
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FEI # 2124215 Boston Scientific CRM Corp
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