-
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes recall
FDA
· Physio-Control, Inc. · Class II
-
Raz-AT (Attendant Tilt) Mobile Shower Commode Chair recall
FDA
· Raz Design Inc · Class II
-
C2O Coconut Water with Pulp (17.5 oz) 15 Pack recall
FDA
· Novamex · Class III
-
Gelsoft Plus recall
FDA
· Vascutek, Ltd. · Class II
-
STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model recall
FDA
· Diagnostica Stago, Inc. · Class II
-
AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model recall
FDA
· Aesculap Inc · Class II
-
Campy CVA Medium 100/PK, R01272 recall
FDA
· Remel, Inc · Class II
-
MRI LED Mobile Exam Light Battery recall
FDA
· MRIMed Inc. · Class II
-
Hitachi Proton Beam Therapy recall
FDA
· Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha · Class II
-
Hitachi Proton Beam Therapy System Ref: PROBEAT-FR recall
FDA
· Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha · Class II
-
NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS:… recall
FDA
· Navitas, LLC. · Class I
-
Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt recall
FDA
· Koi Koi Trading · Class I
-
Fish Ball, Frozen, 20 pieces per pack, 400g Wt recall
FDA
· Koi Koi Trading · Class I
-
Fish Ball, Frozen, 40 pieces per pack, 200g Wt recall
FDA
· Koi Koi Trading · 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
-
IQF frozen Blueberry (30lbs recall
FDA
· Oregon Potato Company LLC · Class I
-
Prime Food Processing Dried Croaker Fish recall
FDA
· Prime Food Processing LLC. · Class I
-
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
-
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep… recall
FDA
· Pure Solutions, Inc. · Class II
-
The Tuna Salad product container is mislabeled with a Chicken Salad lid… recall
FDA
· Reser's Fine Foods, Inc. · Class I
-
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
-
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
-
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