-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
Vios Monitoring System Bedside Monitor Model BSM2050 recall
FDA
· Murata Vios, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Paradigm insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Paradigm insulin pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Paradigm recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Medtronic Pipeline Vantage Embolization Device with Shield Technology recall
FDA
· Micro Therapeutics, Inc. · Class I
-
Medtronic Pipeline Vantage Embolization Device with Shield Technology recall
FDA
· Micro Therapeutics, Inc. · Class I
-
BD Alaris Pump Module recall
FDA
· CareFusion 303, Inc. · Class II
-
139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI… recall
FDA
· CareFusion 303, Inc. · Class II
-
139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS MEDFLEX MN… recall
FDA
· CareFusion 303, Inc. · Class II
-
155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK MINI… recall
FDA
· CareFusion 303, Inc. · Class II
-
138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI… recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis MedFlex 2.0 recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis: MedFlex recall
FDA
· CareFusion 303, Inc. · Class II
-
Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2… recall
FDA
· Nestle-USA, Inc. (Corporate Office) · Class I
-
Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple… recall
FDA
· Nestle-USA, Inc. (Corporate Office) · Class I
-
3M V.A.C. VIA Negative Pressure Wound Therapy System recall
FDA
· Kci USA, Inc. · Class II
-
3M Prevena Plus 125 Therapy Unit and System Kits recall
FDA
· Kci USA, Inc. · Class II
-
Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests… recall
FDA
· HF Acquisition Co LLC · Class II
-
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use… recall
FDA
· Max Mobility LLC · Class I
-
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use… recall
FDA
· Max Mobility LLC · Class I
-
Nestle Toll House Valentine's Chocolate Chip cookie dough, Makes 20 cookies recall
FDA
· Target · Class II
-
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number… recall
FDA
· Medicrea International · Class II
-
Temporary Titanium Abutments recall
FDA
· DDS Lab · Class II
-
ETHIBOND EXCEL Polyester Suture recall
FDA
· Ethicon, LLC · Class II
-
PERMA-HAND Silk Suture recall
FDA
· Ethicon, LLC · Class II
-
PROLENE Polypropylene Suture recall
FDA
· Ethicon, LLC · Class II
-
The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of… recall
FDA
· Hologic, Inc · Class II
-
BD Pyxis MedStation ES AUX Tower recall
FDA
· CareFusion 303, Inc. · Class II
-
Medtronic PIN, 100mm STERILE PERCUTANEOUS recall
FDA
· Medtronic Navigation, Inc. · Class II
-
BD PCR Cartridges used with MAX System recall
FDA
· Becton Dickinson & Co. · Class II
-
Marketside, BROCCOLI FLORETS, 12oz, BEST IF USED BY DEC 10 2024… recall
FDA
· Braga Fresh Foods LLC · Class I
-
8MM, Small Graptor recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM, Tenaculum Forceps recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,FORCE BIPOLAR,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,LONG BIPOLAR GRASPER,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,CURVED BIPOLAR DISSECTOR,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,MEGA SUTURECUT ND,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,LARGE SUTURECUT NEEDLE DRIVER,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,FENESTRATED BIPOLAR FORCEPS,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,COBRA GRASPER,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,MARYLAND BIPOLAR FORCEPS,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,MICRO BIPOLAR FORCEPS,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,PROGRASP FORCEPS,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,CADIERE FORCEPS,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,LONG TIP FORCEPS,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,FORCE BIPOLAR,IS4000 recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,HORIZON SMALL CLIP APPLIER,IS4000¿ recall
FDA
· Intuitive Surgical, Inc. · Class II
-
8MM,TIP-UP FENESTRATED GRASPER,IS4000¿ recall
FDA
· Intuitive Surgical, Inc. · Class II