-
AMSCO 7053HP Washer/Disinfector Model recall
FDA
· Steris Corporation · Class II
-
AMSCO 7052HP Washer/Disinfector Model recall
FDA
· Steris Corporation · Class II
-
BD InLay Optima Ureteral Stent Kit Size: 8 Fr recall
FDA
· C.R. Bard Inc · Class II
-
BD InLay Optima Ureteral Stent Kit Size: 6 Fr recall
FDA
· C.R. Bard Inc · Class II
-
BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr recall
FDA
· C.R. Bard Inc · Class II
-
Bard InLay Optima Size: 6 Fr recall
FDA
· C.R. Bard Inc · Class II
-
Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3"… recall
FDA
· Medline Industries, LP · Class II
-
Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3"… recall
FDA
· Medline Industries, LP · Class II
-
Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3"… recall
FDA
· Medline Industries, LP · Class II
-
Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3"… recall
FDA
· Medline Industries, LP · Class II
-
Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3"… recall
FDA
· Medline Industries, LP · Class II
-
Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3"… recall
FDA
· Medline Industries, LP · Class II
-
CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box… recall
FDA
· Medline Industries, LP · Class II
-
ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full… recall
FDA
· Cardinal Health 200, LLC · Class II
-
CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer… recall
FDA
· Orthofix U.S. LLC · Class III
-
Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model recall
FDA
· Orthofix U.S. LLC · Class III
-
FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model recall
FDA
· Orthofix U.S. LLC · Class III
-
Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System… recall
FDA
· Orthofix U.S. LLC · Class III
-
FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model recall
FDA
· Orthofix U.S. LLC · Class III
-
CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer… recall
FDA
· Orthofix U.S. LLC · Class III
-
Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component… recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Access 2 Reaction Vessels, individual, disposable… recall
FDA
· Beckman Coulter, Inc. · Class II
-
Safe-T-Centesis 6 Fr Catheter Drainage Tray recall
FDA
· Bard Peripheral Vascular Inc · Class II
-
MEDLINE PERFUSION SYRINGE recall
FDA
· Medline Industries, LP · Class II
-
Senographe Pristina, Pristina Serena, and Pristina Serena 3D… recall
FDA
· GE Medical Systems, LLC · Class II
-
Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20… recall
FDA
· Philips North America Llc · Class II
-
ErgoStar CM 60, Model recall
FDA
· Draeger, Inc. · Class I
-
ErgoStar CM 55, Model recall
FDA
· Draeger, Inc. · Class I
-
ErgoStar CM 45, Model recall
FDA
· Draeger, Inc. · Class I
-
ErgoStar CM 40 Model recall
FDA
· Draeger, Inc. · Class I
-
Reagent Kits/ containing flow cells, components of NextSeq 550Dx… recall
FDA
· Illumina, Inc. · Class II
-
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841 recall
FDA
· Philips Ultrasound, Inc · Class II
-
CT 5300; Software Version Number: 4.5, 5.0, 5.1 recall
FDA
· Philips North America Llc · Class II
-
Incisive CT recall
FDA
· Philips North America Llc · Class II
-
Hemochron Activated Clotting Time Low-Range Test Cuvette recall
FDA
· Accriva Diagnostics, Inc. · Class II
-
MAMMOMAT Fusion recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
MAMMOMAT Inspiration recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
MAMMOMAT Revelation recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
KWIK-STIK, Quality control kit for culture media… recall
FDA
· Microbiologics Inc · Class II
-
Olympus OER-Mini recall
FDA
· Aizu Olympus Co., Ltd. · Class II
-
Olympus OER-Pro recall
FDA
· Aizu Olympus Co., Ltd. · Class II
-
Olympus OER-Elite recall
FDA
· Aizu Olympus Co., Ltd. · Class II
-
Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail recall
FDA
· Paragon 28, Inc. · Class II
-
IntelliVue Patient Monitor MX850. Product Number: 866470 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX800. Product Number: 865240 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX750. Product Number: 866471 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX700. Product Number: 865241 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX600. Product Number: 865242 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX550. Product Number: 866066 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX500. Product Number: 866064 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX450. Product Number: 866062 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX400. Product Number: 866060 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX100. Product Number: 867033 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Multi-Measurement Module X3. Product Number: 867030 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Multi Measurement Server X2. Product Number: M3002A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP90. Product Number: M8010A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP80. Product Number: M8008A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP70. Product Number: M8007A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP60. Product Number: M8005A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP50. Product Number: M8004A recall
FDA
· Philips North America Llc · Class II