-
MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer… recall
FDA
· Stryker Corporation · Class II
-
MONARCH Platform, Bronchoscopy recall
FDA
· Auris Health, Inc · Class II
-
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue… recall
FDA
· Bard Peripheral Vascular Inc · Class II
-
The Tuna Salad product container is mislabeled with a Chicken Salad lid… recall
FDA
· Reser's Fine Foods, Inc. · Class I
-
da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000… recall
FDA
· Intuitive Surgical, Inc. · Class II
-
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
FDA
· Alphatec Spine, Inc. · Class II
-
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
FDA
· Alphatec Spine, Inc. · Class II
-
Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
FDA
· Elekta, Inc. · Class II
-
Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
FDA
· Elekta, Inc. · Class II
-
CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g)… recall
FDA
· Ventura Foods LLC · Class II
-
CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/GRAPE JELLY NET WT 1 OZ (28g)… recall
FDA
· Ventura Foods LLC · Class II
-
CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS… recall
FDA
· Ventura Foods LLC · Class II
-
Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz recall
FDA
· Domino Foods Inc · Class III
-
Red Button Movie House Popcorn Pack Size: 24 oz recall
FDA
· Lee's Commissary · Class II
-
Sonic Tots, item number SON00543. Frozen potato product is packaged in… recall
FDA
· McCain Foods USA Inc · Class II
-
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A… recall
FDA
· McCain Foods USA Inc · Class II
-
Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel… recall
FDA
· Costco Wholesale Corporation · Class I
-
Lumipulse ¿-Amyloid Plasma Controls Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse pTau 217 Plasma Controls Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G pTau 217 Plasma Calibrators Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple… recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical 25GA Backflush, VS0270.25 recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical TID Pharos Illuminated Depressor, VS0801B recall
FDA
· Vortex Surgical Inc. · Class II
-
Rumex Disposable Diamond Dusted ILM Elevator, 12-7523 recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical I2 Injection Kit, VS0500 recall
FDA
· Vortex Surgical Inc. · Class II
-
Tecfen Retractable Membrane Polisher, QTPR1267-23 recall
FDA
· Vortex Surgical Inc. · Class II