-
REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
REF: 382544 BD Insyte Autoguard Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
REF: 381811, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
REF: 382944, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
REF: 381433, BD Insyte Autoguard Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
REF: 381533, BD Insyte Autoguard Winged, Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
REF: 382633, BD Insyte Autoguard BC Winged… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
REF: 381423, BD Insyte Autoguard, Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311… recall
FDA
· Balt USA, LLC · Class II
-
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875… recall
FDA
· Balt USA, LLC · Class II
-
Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle recall
FDA
· The Coca-Cola Company · Class II
-
BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP recall
FDA
· Bd Switzerland Sarl · Class II
-
BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP recall
FDA
· Bd Switzerland Sarl · Class II
-
BD Texium: 3 mL recall
FDA
· Bd Switzerland Sarl · Class II
-
BD Texium Needle-Free Syringe: 3 mL recall
FDA
· Bd Switzerland Sarl · Class II
-
Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium… recall
FDA
· Bd Switzerland Sarl · Class II
-
Allon 2001. Part Number: 200-00263 recall
FDA
· Belmont Instrument LLC · Class II
-
Newport HT70 Ventilator recall
FDA
· Covidien, LP · Class I
-
Sample probe sucks a sample dispensed into a tube or cup and discharges… recall
FDA
· Beckman Coulter Mishima K.K. · Class II
-
Sample probe sucks a sample dispensed into a tube or cup and discharges… recall
FDA
· Beckman Coulter Mishima K.K. · Class II
-
GNC Women's 30+ Vitapak, Carton of 30 Sachets recall
FDA
· GNC Holdings LLC · Class III
-
Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen recall
FDA
· Cardinal Health 200, LLC · Class II
-
Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumen recall
FDA
· Cardinal Health 200, LLC · Class II
-
Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen recall
FDA
· Cardinal Health 200, LLC · Class II
-
Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen recall
FDA
· Cardinal Health 200, LLC · Class II
-
Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen recall
FDA
· Cardinal Health 200, LLC · Class II
-
Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5… recall
FDA
· Cardinal Health 200, LLC · Class II
-
ADVIA Centaur HCY Calibrator (2 Pack) recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
Atellica IM Homocysteine Calibrator (2 Pack) recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM recall
FDA
· Smith & Nephew, Inc. · Class II
-
Centerline Biomedical IOPS Guidewire 2 recall
FDA
· Centerline Biomedical Inc · Class I
-
Bard¿ Single Intragastric Linton Balloon Tube recall
FDA
· C.R. Bard Inc · Class I
-
Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) recall
FDA
· C.R. Bard Inc · Class I
-
Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) recall
FDA
· C.R. Bard Inc · Class I
-
Bard Blakemore Esophageal-Nasogastric Tube (Adult) recall
FDA
· C.R. Bard Inc · Class I
-
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube recall
FDA
· C.R. Bard Inc · Class I
-
Philips Tempus Pro Patient Monitor recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II
-
Enhanced Verify Evaluation Handset (CFN HH90130FA) recall
FDA
· Medtronic Neuromodulation · Class II
-
Quantum Informatics - VISION / LIVE VUE Product Name: Monitor… recall
FDA
· Spectrum Medical Ltd. · Class II
-
Quantum Informatics - VIPER Product Name: Monitor, Physiological… recall
FDA
· Spectrum Medical Ltd. · Class II
-
Straight Inflow/Bifurcated Outflow Line Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Straight Inflow/Outflow Patient Line Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Hyperthermia Pump Procedure Kit recall
FDA
· Belmont Instrument LLC · Class II
-
DxC 500 AU Clinical Chemistry Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP… recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II
-
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount recall
FDA
· Ihb Operations B.V. · Class II
-
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090… recall
FDA
· Radiometer Medical ApS · Class II
-
InPen smart insulin pen recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Merit Medical recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical recall
FDA
· Merit Medical Systems, Inc. · Class II
-
BD PYXIS MEDBANK (Name recall
FDA
· CareFusion 303, Inc. · Class II
-
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 recall
FDA
· Medtronic Xomed, Inc. · Class II
-
HeartMate Mobile Power Unit recall
FDA
· Thoratec LLC · Class I
-
AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform… recall
FDA
· ZOLL Circulation, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I