686 articles — Page 31 of 35
FDA recall notice for Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augment, REF 1122370, Sterile, a component of the Unity Total Kne
FDA recall notice for Corin Unity Knee Patella, Size 3 / 8.5mm, Centered Dome 3 PEG-UHMWPE, REF 112.018.06, Sterile, a component of the Unity Total Knee System.
FDA recall notice for Corin TriFit TS, Size 8, Standard Tapered Stem, REF 694.0008, Sterile. (Corin Ltd). Reason: The packaging system on the devices have poten
FDA recall notice for Corin MetaFix Hip Stem, Size 1, Short Neck, 135 degrees, Collared Hip Stem, REF 579.0201, Sterile. (Corin Ltd). Reason: The packaging syst
FDA recall notice for Corin BIOLOX Delta Mod Head, diameter 28mm Medium 0mm, 12/14 Taper, REF 104.2805, Sterile, a component of the Trinity Acetabular System. (
FDA recall notice for Corin Unity Knee CS Insert, Size 5 / 9.0mm, Fixed Condylar Stabilised - UHMWPE, REF 1125182, Sterile, and Corin Unity Knee CS Insert, Siz
FDA recall notice for smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during orthopedic surgery. (Smith & Nephew Orthopaedics Ltd. (Aur
FDA recall notice for The Instructions for Use (IFU) for: Gelsoft Plus Bifurcate, Gelsoft Plus Ax-Fem, GelsoftPlus ERS Ax-Fem, Gelweave Straight, Gelweave Trif
FDA recall notice for Simpleware ScanIP medical software. For transfer of imaging information from a medical scanner to an output file, and for simulating/eval
FDA recall notice for Simpleware ScanIP software. For transfer of imaging information from a medical scanner to an output file, and for simulating/evaluating su
FDA recall notice for Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte specific reagents (ASR's) (Cytocell Ltd.). Reason: May show une
FDA recall notice for Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. Produc
FDA recall notice for Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator, SAM 360P fully automatic defibrillator, SAM 500P semi-automatic defibril
FDA recall notice for Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor (SUREPULSE MEDICAL LTD). Reason: Retroactively reporte
FDA recall notice for Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor (SUREPULSE MEDICAL LTD). Reason: Retroactively reported
FDA recall notice for Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215 (Corin Ltd). Reason: The BIOLOX Delta Ceramic Head size 36XL is labelled as
FDA recall notice for Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615 (Corin Ltd). Reason: The BIOLOX Delta Ceramic Head size 36XL is labelled as
FDA recall notice for CytoCell BCL11B Distal in Texas Red Spectrum- Analyte Specific Reagent Ref: MPD39782 (Cytocell Ltd.). Reason: An error with the chromomap
FDA recall notice for NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176 (Thor Photomedicine Ltd). Reason: Failure of ball stud components causing t
FDA recall notice for NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183 (Thor Photomedicine Ltd). Reason: Failure of ball stud components c