-
Bellabu Bear Recalls Children's Robes Due to Burn Hazard; Violates Mandatory Standards for Children's Sleepwear
CPSC
· Bellabu Bear
-
Tempo USA Recalls Ambiano Electric Pressure Cookers Due to Serious Burn Hazard, Multiple Burn Injuries Reported; Sold at ALDI
CPSC
· Tempo USA
-
Calico Brands Recalls Scripto Premium Torches Due to Risk of Injury or Death from Fires and Burns…
CPSC
· Calico Brands
-
Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0… recall
FDA
· MedicalCommunications GmbH · Class II
-
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031… recall
FDA
· Schiller, Ag · Class II
-
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P recall
FDA
· Medline Industries, LP · Class I
-
MAGNETOM Vida Fit recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Vida (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio Dot Upgrade recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio Dot recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Spectra as the following: 1. MAGNETOM Spectra recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra Fit BioMatrix recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra fit recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Prisma recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Lumina (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Connectom.X. Model Number: 11371480 recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Cima.X (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
BIOGRAPH One (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
Biograph mMR. Model Number: 10433372 recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
ZAP-X Radiosurgery System, Model: 300150 recall
FDA
· Zap Surgical Systems · Class II
-
Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to… recall
FDA
· Bard Peripheral Vascular Inc · Class II
-
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) recall
FDA
· North American Rescue LLC. · Class II
-
Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers… recall
FDA
· Medline Industries, LP · Class I
-
Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616, (2) AG 630… recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
Change Healthcare Radiology Solutions software version 14.2.2 recall
FDA
· Change Healthcare Canada Company · Class II
-
NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
IMPLANT EPIKUT PLUS MT16 3,5X10,0MM recall
FDA
· S.I.N. Implant System Ltda · Class II
-
Getinge 88-Series Washer- Disinfector recall
FDA
· Getinge Disinfection Ab · Class II
-
Cardio Vascular-Allura Centron recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper CV20 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 FD20/15 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 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10C recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 5 mL, Rx Only, Sterile… recall
FDA
· Apotex Corp. · Class II
-
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5%… recall
FDA
· Apotex Corp. · Class II
-
Carbamazepine Extended-Release Tablets, USP 400 mg… recall
FDA
· Amerisource Health Services LLC · Class II
-
Entecavir Tablets, USP, 1 mg, 30-count bottle, Rx Only… recall
FDA
· Zydus Pharmaceuticals (USA) Inc · Class II