15 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems-IVD intended for targeted sequencing of human genomic DNA (gDNA) from peripheral whole-blood samples and DNA and RNA extracted from formalin-fixed, paraffin-embedded (FFPE) samples. The Ion PGM Dx Instrument System is not intended for whole genome or de novo sequencing Product Name Installer /SKU /Updater SKU: (1) Torrent Suite Dx Software 5.14 -A52422/ A52417 (2) Torrent Suite Dx Software 5.12.5- A46166/ A46167 (3)Torrent Suite Dx Software 5.8- A36601/ A36602 (4)Torrent Suite Dx Software 5.6.4- A33178/ A33178 (5)Torrent Suite Dx Software 5.0- A29166/ A29166
FDA Recall
Open, Classified
·Life Technologies Corporation·Product code PFF·February 7, 2024
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, 5C4482
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, REF R5C4482
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short, 5C4483
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, REF R5C4482E
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter MiniCap Extended Life PD Transfer Set Twist Clamp - Extra Short, REF R5C4483
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, 5C4482EJ
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Long, REF R5C4484
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter MiniCap Extended Life PD Transfer Set (Easy-Lock), 5C4449
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Various products which were contract sterilized.
FDA Recall
Open, Classified
·Anewmed Corporation·Product code DQX·May 23, 2019
Baxter CAPD System Transfer Set (CAPD MiniCap Transfer Set II (24cm)), Code No. T5C4482
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter Equipo de transferencia para DP MiniCap de vida util prolongada con pinza de torsion, 5C4482S
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
Baxter CAPD System Transfer Set (CAPD MiniCap Transfer Set II (34cm)), Code No. T5C4484
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code KDJ·January 7, 2022
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).
FDA Recall
Open, Classified
·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code ISA·April 9, 2025
Superion Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm
FDA Recall
Open, Classified
·Boston Scientific Neuromodulation Corporation·Product code NQO·October 12, 2022