-
Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle recall
FDA
· Flexicare Medical (Dongguan) Ltd. · Class I
-
BritePro Solo Mini with Pro Miller Blade Size 1.5 recall
FDA
· Flexicare Medical (Dongguan) Ltd. · Class I
-
BritePro Solo Single-Use Fiber Optic Handle and Blade Refs: 040-331U (Mac… recall
FDA
· Flexicare Medical (Dongguan) Ltd. · Class I
-
BritePro Solo Single-Use Fiber Optic Mini Handle and Blade Ref:… recall
FDA
· Flexicare Medical (Dongguan) Ltd. · Class I
-
BD Alaris Pump Infusion Sets recall
FDA
· CareFusion 303, Inc. · Class I
-
BD Alaris Pump Module Model, 8100 with Guardrails… recall
FDA
· CareFusion 303, Inc. · Class I
-
Plum Duo Infusion System, List Number: 400020401 recall
FDA
· ICU Medical, Inc. · Class I
-
Queen Bee Gardens Whipped Honey Huckleberry Intended use: spread recall
FDA
· Queen Bee Gardens · Class II
-
Queen Bee Gardens Whipped Honey Pure recall
FDA
· Queen Bee Gardens · Class II
-
Queen Bee Gardens Whipped Honey Raspberry recall
FDA
· Queen Bee Gardens · Class II
-
Spironolactone Tablets, USP, 25 mg, 100-count bottle, Rx only, Mfg recall
FDA
· Sun Pharmaceutical Industries Inc · Class II
-
RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only… recall
FDA
· Cardinal Health Inc. · Class II
-
Xolair (omalizumab injection), 75 mg/0.5 ml, Rx only, Genentech, Inc… recall
FDA
· Cardinal Health Inc. · Class II
-
Xolair (omalizumab injection), 150 mg/ml, 1 auto-injector, Rx only… recall
FDA
· Cardinal Health Inc. · Class II
-
Duloxetine D/R, 30 mg, 30 Caps, RX Only, Packaged as a) 30-count bottle recall
FDA
· Direct Rx · Class II
-
Duloxetine D/R, 20 mg, 30 Caps, 30-count bottle, RX Only… recall
FDA
· Direct Rx · Class II
-
Doxepin Hydrochloride Capsules, USP, 10 mg, 100 Capsules, Rx only… recall
FDA
· Alembic Pharmaceuticals Limited · Class II
-
Duloxetine Delayed-Release Capsules, USP, 60mg, 1,000-count bottles… recall
FDA
· Breckenridge Pharmaceutical, Inc. · Class II
-
La Ligne Recalls Enfant Bonne Nuit Pajamas Due to Burn Hazard; Violates Mandatory Flammability Standards
CPSC
· La Ligne
-
Fieldsheer Apparel Technologies Recalls Heated Socks Due to Injury Hazard
CPSC
· Fieldsheer Apparel Technologies
-
Petmate Recalls Pet Zone Pet Toys Due to Risk of Serious Injury or Death from Ingestion Hazard…
CPSC
· Petmate
-
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port… recall
FDA
· Fresenius Kabi USA, LLC · Class II
-
LVP Primary Administration Set, Single Outlet Low Sorbing (Qty 25) recall
FDA
· Fresenius Kabi USA, LLC · Class II
-
LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site… recall
FDA
· Fresenius Kabi USA, LLC · Class II
-
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port… recall
FDA
· Fresenius Kabi USA, LLC · Class II
-
3M Ranger Irrigation Fluid Warming Set recall
FDA
· 3M Company · Class II
-
RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack) recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
Blood/MacConkey Biplate 100/PK, Product Number R02049 recall
FDA
· Remel, Inc · Class II
-
Blood/EMB, Levine 100/PK, Product Number R02041 recall
FDA
· Remel, Inc · Class II
-
Strep Selective II Agar, Product Number R01859 recall
FDA
· Remel, Inc · Class II
-
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202 recall
FDA
· Remel, Inc · Class II
-
Osteotec Product Name: Osteotec Silicone Finger Implant Model recall
FDA
· Osteotec Limited · Class II
-
Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) recall
FDA
· Volcano Corp · Class II
-
ASPRIRE Cristalle Mammography System (cleared under K212873) installed… recall
FDA
· FUJIFILM Healthcare Americas Corporation · Class II
-
Upgrade to MR 7700 Model Number ( recall
FDA
· Philips North America Llc · Class II
-
SmartPath to Ingenia Elition X Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for XR and 3.0T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for 3.0T Model Number ( recall
FDA
· Philips North America Llc · Class II
-
MR 7700 Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
MR 5300 Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Intera 3.0T Quasar Dual Model Number ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition X Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition S Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition X Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition S Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T CX Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T S Model Number ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 3.0T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 1.5T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Achieva XR recall
FDA
· Philips North America Llc · Class II
-
Achieva 3.0T recall
FDA
· Philips North America Llc · Class II
-
SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no recall
FDA
· Medline Industries, LP · Class II
-
Precision Sampling Set recall
FDA
· Capnia Inc · Class II
-
IontoPatch 80, On-the-Go Patch Therapy, Model recall
FDA
· LTS Therapy Systems, LLC · Class II
-
IontoPatch STAT, On-the-Go Patch Therapy, Model recall
FDA
· LTS Therapy Systems, LLC · Class II
-
LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) recall
FDA
· Microbiologics Inc · Class II
-
LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) recall
FDA
· Microbiologics Inc · Class II
-
Sprinter Cart/Sprinter Cart XL Infusion Pole recall
FDA
· Maquet Cardiopulmonary Gmbh · Class II