-
Alcon Laboratories, Inc recall
FDA
· Alcon Research LLC · Class II
-
Alcon Laboratories, Inc recall
FDA
· Alcon Research LLC · Class II
-
Alcon Laboratories, Inc recall
FDA
· Alcon Research LLC · Class II
-
Preat, Astra EV-compatible 4.2mm Digital Analog recall
FDA
· Preat Corp · Class II
-
Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model recall
FDA
· Neurovision Medical Products Inc · Class II
-
TrueDent White, TDM110, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Yellow, TDM140, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Magenta, TDM130, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Cyan, TDM 120, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Clear, TDM 100, Model No recall
FDA
· Stratasys Ltd · Class III
-
FEM-FLEXII Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
Crown Point Shelled Edamame, net wt recall
FDA
· Alpine Food DIstributing, Inc · Class II
-
VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt recall
FDA
· Face Rock Creamery LLC · Class I
-
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
ADVIA¿ 120/2120/2120i SETpoint Calibrator recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
REF: 666289 , BD FACS, 7-Color Setup Beads, 25 Runs, CE, IVD… recall
FDA
· Becton, Dickinson and Company, BD Bio Sciences · Class II
-
REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only… recall
FDA
· Becton, Dickinson and Company, BD Bio Sciences · Class II
-
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra recall
FDA
· C.R. Bard Inc · Class II
-
BD Heyman Follower Coude Tip for following sizes: 12Fr recall
FDA
· C.R. Bard Inc · Class II
-
BD Heyman Follower Straight Tip for following sizes: 10Fr recall
FDA
· C.R. Bard Inc · Class II
-
Change Healthcare Cardiology Hemodynamics Software recall
FDA
· Change Healthcare Canada Company · Class II
-
Change Healthcare Cardiology Hemo Software recall
FDA
· Change Healthcare Canada Company · Class II
-
Apex Knee System recall
FDA
· Corin Medical, Ltd. · Class II
-
Valeda Light Delivery System Product Name: Light Based Device for Dry Age… recall
FDA
· Lumithera Inc · Class III
-
Medline convenience kits containing BD Insyte Autoguard Shielded IV… recall
FDA
· Medline Industries, LP · Class II
-
Medline convenience kits containing BD Insyte Autoguard Shielded IV… recall
FDA
· Medline Industries, LP · Class II
-
Medline convenience kits containing BD Insyte Autoguard Shielded IV… recall
FDA
· Medline Industries, LP · Class II
-
HardyCHROM CRE, selective and differential culture medium for… recall
FDA
· Hardy Diagnostics · Class II
-
BiPAP A40 Ventilator recall
FDA
· Philips Respironics, Inc. · Class I
-
BiPAP A30 Ventilators recall
FDA
· Philips Respironics, Inc. · Class I
-
BiPAP V30 Auto Ventilator recall
FDA
· Philips Respironics, Inc. · Class I
-
Shell Eggs recall
FDA
· August Egg Company · Class I
-
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an… recall
FDA
· Peak Cocktails · Class II
-
Spectral CT. Computed tomography X-ray system recall
FDA
· Philips North America Llc · Class II
-
REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487 recall
FDA
· Beckman Coulter, Inc. · Class II
-
BD BACTEC MGIT 960 PZA Kit recall
FDA
· Becton Dickinson & Co. · Class II
-
CDI OneView System BPM Probe: Cat recall
FDA
· Terumo Cardiovascular Systems Corporation · Class II
-
Product Name [ recall
FDA
· CareFusion 303, Inc. · Class II
-
REF: 381434 BD Insyte Autoguard Shielded IV Catheter… recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
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
-
DxI 9000 Access Immunoassay Analyzer C11137 recall
FDA
· Beckman Coulter, Inc. · Class II
-
ICU Medical Plum Solos, Item number 400011001 recall
FDA
· ICU Medical, Inc. · Class II
-
ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001… recall
FDA
· ICU Medical, 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
-
Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment recall
FDA
· Preat Corp · Class II