-
Intraocular Lens recall
FDA
· Bausch & Lomb Surgical, Inc. · Class I
-
Intraocular lens recall
FDA
· Bausch & Lomb Surgical, Inc. · Class I
-
DxC 500 AU Clinical Chemistry Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
GE Healthcare CARESTATION 750c A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 750c A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 750 A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 750 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650c A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650C A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650C A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650 SE, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650 A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 620 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 620 SE, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 620 A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 620 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
Rover Product Name: Mobile X-ray System Model recall
FDA
· Micro-X Ltd. · Class II
-
Rover Product Name: Mobile X-ray System Model recall
FDA
· Micro-X Ltd. · Class II
-
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430… recall
FDA
· Philips North America Llc · Class II
-
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090… recall
FDA
· Radiometer Medical ApS · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 recall
FDA
· Medtronic Xomed, Inc. · Class II
-
Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION… recall
FDA
· Channel Medsystems, Inc. · Class II
-
Rover Product Name: Mobile X-ray System Model recall
FDA
· Micro-X Ltd. · Class II
-
Rover Product Name: Mobile X-ray System Model recall
FDA
· Micro-X Ltd. · Class II
-
Maquet VH-3010 Power Supply recall
FDA
· Maquet Cardiovascular, LLC · Class II
-
Stimulation RC Clinician Programmer Application, Model A71400… recall
FDA
· Medtronic Neuromodulation · Class II
-
DxC 500 AU Clinical Chemistry Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
A820 myPTM Software Application associated with Medtronic SynchroMed Pump… recall
FDA
· Medtronic Neuromodulation · Class II
-
Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml… recall
FDA
· Bioriginal Food & Science Corporation · Class II
-
chlorproMAZINE Hydrochloride Tablets, USP 100 mg, Rx Only… recall
FDA
· Glenmark Pharmaceuticals Inc., USA · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
BD Pyxis: Anesthesia Station ES recall
FDA
· CareFusion 303, Inc. · Class II
-
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture recall
FDA
· Stryker 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
-
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
-
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
-
Numerous models of nonsterile hemostatic forceps: (1) recall
FDA
· Aesculap Inc · Class II
-
Numerous models of nonsterile hemostatic forceps: (1) recall
FDA
· Aesculap Inc · Class II
-
Numerous models of nonsterile hemostatic forceps: (1) recall
FDA
· Aesculap Inc · Class II