-
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
-
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
-
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
-
MiniMed 780G Insulin Pump recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
CellMek SPS Sample Preparation System recall
FDA
· Beckman Coulter, Inc. · Class II
-
EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H recall
FDA
· Encore Medical, LP · Class II
-
EMPOWR 3D Knee Tibial Insert 5R 14MM, VE recall
FDA
· Encore Medical, LP · Class II
-
Da Vinci Product Name: da Vinci X, Xi Surgical System… recall
FDA
· Intuitive Surgical, Inc. · Class II
-
COULTER DxH Diluent recall
FDA
· Beckman Coulter, Inc. · Class II
-
JUICE from the Raw, cashew coffee milk recall
FDA
· Everpress Juice · Class I
-
JUICE from the Raw, cashew milk recall
FDA
· Everpress Juice · Class I
-
JUICE from the Raw, spicy lemonade recall
FDA
· Everpress Juice · Class I
-
JUICE from the Raw, upbeat recall
FDA
· Everpress Juice · Class I
-
JUICE from the Raw, pineapple mint recall
FDA
· Everpress Juice · Class I
-
JUICE from the Raw, sweet greens recall
FDA
· Everpress Juice · Class I
-
JUICE from the Raw, DETOX GREENS recall
FDA
· Everpress Juice · Class I
-
BEAR Implant recall
FDA
· Miach Orthopaedics · Class II
-
Conductivity Standard Solution recall
FDA
· NIPRO Technical Services, Inc. · Class II
-
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recall
FDA
· Cerapedics, Inc. · Class II
-
Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap… recall
FDA
· Quten Research Institiute LLC · Class II
-
SQ40S Blood Transfusion Filter recall
FDA
· GVS TM, Inc · Class II
-
The LDL-Cholesterol assay is comprised of two distinct phases recall
FDA
· Beckman Coulter Ireland, Inc. · Class II
-
Ion Endoluminal System Product Name: Ion Vision Probe Bag Model recall
FDA
· Intuitive Surgical, Inc. · Class II
-
MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model recall
FDA
· MicroPort Orthopedics Inc. · Class II
-
Allwell Angioplasty Pack recall
FDA
· Merit Medical Systems, Inc. · Class II