-
Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL… recall
FDA
· Encore Medical, LP · Class II
-
EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model recall
FDA
· Encore Medical, LP · Class II
-
Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT… recall
FDA
· Encore Medical, LP · Class II
-
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
-
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
-
Red Button Movie House Popcorn Pack Size: 24 oz recall
FDA
· Lee's Commissary · 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
-
MiniMed 780G Insulin Pump recall
FDA
· Medtronic MiniMed, 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
-
WinCo Foods Deli Margherita Pizza Thin Crust, Item #67279. Net wt recall
FDA
· WinCo Foods LLC · Class II
-
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recall
FDA
· Cerapedics, 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
-
Allwell Angioplasty Pack recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical , Custom Procedure Kit Reference Numbers: K12T-04270A… recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical , Custom Manifold Kit recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical , Custom Inflation Kit recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical , Custom Waste Management Kit Vascular Tray recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Allwell Inflation Device, for angiographic use recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference… recall
FDA
· Merit Medical Systems, Inc. · Class II