-
Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2)… recall
FDA
· International Life Sciences · Class II
-
Artelon FlexBand Plus Ref: 41054 & 41057 recall
FDA
· International Life Sciences · Class II
-
Artelon FlexBand Dynamic Matrix Ref: 31057 recall
FDA
· International Life Sciences · Class II
-
APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model recall
FDA
· Medartis AG · Class II
-
APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model recall
FDA
· Medartis AG · Class II
-
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes recall
FDA
· Physio-Control, Inc. · Class II
-
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients:… recall
FDA
· Palmetto Gourmet Foods Inc. · Class II
-
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients:… recall
FDA
· Palmetto Gourmet Foods Inc. · Class II
-
Gelsoft Plus recall
FDA
· Vascutek, Ltd. · Class II
-
PIE PAK Models: P2HC-A, P2HC-S, P2HC recall
FDA
· Edermy LLC · Class II
-
PIE Trolley System Model: 2005 recall
FDA
· Edermy LLC · Class II
-
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
-
MRI LED Mobile Exam Light Battery recall
FDA
· MRIMed Inc. · Class II
-
NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS:… recall
FDA
· Navitas, LLC. · Class I
-
Yoyo Gummy Grape Plus Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
FDA
· Sb Food LLC · Class II
-
Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
FDA
· Sb Food LLC · Class II
-
Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
FDA
· Sb Food LLC · 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
-
Private Label CVS. Model Number: CVS405406… recall
FDA
· Integra LifeSciences Corp. (NeuroSciences) · Class II
-
MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY… recall
FDA
· Integra LifeSciences Corp. (NeuroSciences) · Class II
-
MediHoney Gel with Active Leptospermum Honey recall
FDA
· Integra LifeSciences Corp. (NeuroSciences) · Class II
-
Teslatome Bipolar Sphincterotomes recall
FDA
· Wilson-Cook Medical Inc. · Class II
-
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep… recall
FDA
· Pure Solutions, Inc. · Class II
-
Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
CPSC
· Meijer
-
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
-
Spectral CT 7500 on Rails recall
FDA
· Philips North America Llc · Class II
-
Spectral CT recall
FDA
· Philips North America Llc · Class II
-
IQon Spectral CT recall
FDA
· Philips North America Llc · Class II
-
Brilliance iCT recall
FDA
· Philips North America Llc · 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
-
Spicy Breakfast Burrito in a flour tortilla recall
FDA
· MG Foods-Compass Group · Class II
-
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