-
Entecavir Tablets, USP, 0.5 mg, 30-count bottle, Rx Only… recall
FDA
· Zydus Pharmaceuticals (USA) Inc · Class II
-
In Motion Design Recalls Evermore Surprise Eggs Due to Risk of Serious Injury; Violates Federal Lead Content Ban
CPSC
· In Motion Design
-
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No recall
FDA
· Maquet Cardiovascular, LLC · Class II
-
Allura CV20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane OR Table Product Codes: (1)722020, (2) 722025 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 Product Codes: (1)722011, (2) 722027, (3) 722005 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
BeneVision N1 Patient Monitor (N1) recall
FDA
· Mindray North America · Class II
-
Chromophare Surgical Light System recall
FDA
· Stryker Communications · Class II
-
Juggerknot Mini Soft Anchors, Model recall
FDA
· Biomet, Inc. · Class II
-
Extractor Pro RX Retrieval Balloon Catheter recall
FDA
· Boston Scientific Corporation · Class II
-
Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight recall
FDA
· Ortoma Ab · Class II
-
FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative, multiplexed… recall
FDA
· Biofire Defense · Class II
-
Voyant 1-Day Premium Toric, (stenfilcon A) contact lens recall
FDA
· CooperVision, Inc. · Class II
-
Sofmed Breathables, (stenfilcon A) contact lens recall
FDA
· CooperVision, Inc. · Class II
-
MyDay Toric, stenfilcon A) Contact Lens recall
FDA
· CooperVision, Inc. · Class II
-
STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device… recall
FDA
· Ethicon, LLC · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Baster Continu-Flo Solution Set, Non-Vented… recall
FDA
· Baxter Healthcare Corporation · Class II
-
Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label… recall
FDA
· Extract Labs, Inc. · Class II
-
Blue Razz 20mg Gummies Brand Name: None - unlabeled bulk (private-label… recall
FDA
· Extract Labs, Inc. · Class II
-
Elderberry 20mg Gummies Brand Name: None - unlabeled bulk (private-label… recall
FDA
· Extract Labs, Inc. · Class II
-
Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name:… recall
FDA
· Extract Labs, Inc. · Class II
-
READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic… recall
FDA
· Medline Industries, LP · Class III
-
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate… recall
FDA
· Granules Pharmaceuticals Inc. · Class III
-
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate… recall
FDA
· Granules Pharmaceuticals Inc. · Class III
-
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate… recall
FDA
· Granules Pharmaceuticals Inc. · Class III
-
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate… recall
FDA
· Granules Pharmaceuticals Inc. · Class III
-
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate… recall
FDA
· Granules Pharmaceuticals Inc. · Class III
-
Azelaic Acid Gel, 15%, 50 grams, For Topical Use Only, Rx only… recall
FDA
· Glenmark Pharmaceuticals Inc., USA · Class II
-
TopCare Health 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can… recall
FDA
· Consumer Product Partners, LLC · Class III
-
Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can… recall
FDA
· Consumer Product Partners, LLC · Class III
-
Mad Rabbit Recalls "RELIEVE" Lidocaine Numbing Cream Due to Risk of Serious Injury or Death from Poisoning to Young Children…
CPSC
· Mad Rabbit
-
AMTRADING Recalls Hoovy Cooling Gel Insert Pads for Car Seats and Strollers Due to Burn Hazard
CPSC
· Amtrading
-
Sunbeam Products Recalls More than One Million Oster French Door Countertop Ovens Due to Burn Hazard
CPSC
· Sunbeam Products
-
SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray recall
FDA
· C.R. Bard Inc · Class II
-
SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control… recall
FDA
· C.R. Bard Inc · Class II
-
SureStep Foley Tray System Bardex I.C. Complete Care Infection Control… recall
FDA
· C.R. Bard Inc · Class II
-
Heartstring III Proximal Seal System, 4.3 MM… recall
FDA
· Maquet Cardiovascular, LLC · Class II
-
Heartstring III Proximal Seal System, 3.8 MM… recall
FDA
· Maquet Cardiovascular, LLC · Class II
-
Heartstring III Proximal Seal System recall
FDA
· Maquet Cardiovascular, LLC · Class II
-
i-STAT EG6+ cartridge recall
FDA
· Abbott Point Of Care Inc. · Class II