-
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate… recall
FDA
· Tyber Medical · Class II
-
A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula… recall
FDA
· Tyber Medical · Class II
-
IntelePACS (Image Fusion Module) - InteleViewer recall
FDA
· Intelerad Medical Systems Incorporated · Class II
-
BD Pyxis MedFlex 2.0 recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis: MedFlex recall
FDA
· CareFusion 303, Inc. · Class II
-
Assorted Chocolate Caramels with kosher sea salt, Net Weight 1.25lb recall
FDA
· V Chocolates, Inc · Class II
-
Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe… recall
FDA
· Turbare Manufacturing · Class II
-
Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton, Rx Only… recall
FDA
· Padagis US LLC · Class II
-
ARVA Recalls NEO BT PRO Avalanche Transceivers Due to Risk of Loss of Emergency Transmission; Risk of Serious Injury or Death
CPSC
· ARVA
-
Kichler Lighting Recalls Wall Sconces Due to Risk of Electric Shock
CPSC
· Kichler Lighting
-
P.J. Salvage Recalls Pajama Sets and Robes Due to Burn Hazard; Violation of Federal Flammability Regulations for Children's Sleepwear…
CPSC
· P.J. Salvage
-
Forever 21 Recalls Children's Pajamas Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold Exclusively by Forever 21
CPSC
· Forever 21
-
Triangle Tube Recalls Prestige and Aerco Esteem Gas Boilers Due to Carbon Monoxide (CO) Poisoning Hazard; Two Deaths Reported
CPSC
· Triangle Tube
-
Dexcom G6, Continuous Glucose Monitoring System recall
FDA
· Dexcom, Inc. · Class II
-
Dexcom G6, Continuous Glucose Monitoring System recall
FDA
· Dexcom, Inc. · Class II
-
Dexcom G6, Continuous Glucose Monitoring System, REFs: STK-OM-001… recall
FDA
· Dexcom, Inc. · Class II
-
remel BLOOD AGAR EMB AGAR BIPLATE recall
FDA
· Remel, Inc · Class II
-
remel BLOOD AGAR MacCONKEY AGAR BIPLATE recall
FDA
· Remel, Inc · Class II
-
Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode… recall
FDA
· Augustine Temperature Management, LLC · Class II
-
Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode… recall
FDA
· Augustine Temperature Management, LLC · Class II
-
Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode… recall
FDA
· Augustine Temperature Management, LLC · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation- Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation -Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation -Intended as a Radiation Therapy Treatment Planning System Model recall
FDA
· Raysearch Laboratories Ab · Class II
-
RayStation Intended as a Radiation Therapy Treatment Planning System recall
FDA
· Raysearch Laboratories Ab · Class II
-
LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO… recall
FDA
· Physio-Control, Inc. · Class II
-
AnchorFast Guard, Oral Endotracheal Tube Fastener recall
FDA
· Hollister Incorporated · Class II
-
AnchorFast, Oral Endotracheal Tube Fastener recall
FDA
· Hollister Incorporated · Class II
-
AnchorFast SlimFit, Oral Endotracheal Tube Fastener recall
FDA
· Hollister Incorporated · Class II
-
AnchorFast Guard Select, Oral Endotracheal Tube Fastener recall
FDA
· Hollister Incorporated · Class II
-
Irix-A Integrated Lumbar Fusion System, Model Number X080-423011-08PC… recall
FDA
· XTANT Medical Holdings, Inc · Class II
-
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
-
Cardio Vascular-Allura Centron recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 7 M20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 7 M12 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 7 B20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 7 B12 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 5 M20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 5 M12 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 3 M15 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Azurion 3 M12 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Allura Xper FD10C recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Allura CV20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I
-
Allura Xper FD20/20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class I