-
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count… recall
FDA
· Medline Industries, LP · Class II
-
Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count… recall
FDA
· Medline Industries, LP · Class II
-
Xhibit Product Name: Xhibit Central Station Model recall
FDA
· Spacelabs Healthcare, Inc. · Class II
-
navify Digital Pathology (on-prem) v2.5, Material Number 10092343001… recall
FDA
· Ventana Medical Systems, Inc. · Class II
-
Atellica CH Urine Albumin recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN:… recall
FDA
· Boston Scientific Corporation · Class II
-
Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions… recall
FDA
· Boston Scientific Corporation · Class II
-
Radial Jaw 4 Standard Capacity Biopsy Forceps with the following… recall
FDA
· Boston Scientific Corporation · Class II
-
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that… recall
FDA
· ResMed Ltd. · Class I
-
Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity… recall
FDA
· Philips Medical Systems · Class II
-
IQon Spectral CT IQon Spectral CT Upgrades recall
FDA
· Philips Medical Systems · Class II
-
Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64… recall
FDA
· Philips Medical Systems · Class II
-
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android) recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Penumbra System RED 68 Reperfusion Catheter recall
FDA
· Penumbra, Inc. · Class II
-
Bone Marrow Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
Arterial Line Kit 20ga x 6 recall
FDA
· Argon Medical Devices, Inc · Class I
-
T-Lok Bone Marrow Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
General Biospy Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
One-Piece Introducer Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall
FDA
· Argon Medical Devices, Inc · Class I
-
OmniTract Surgical Retractor System, which includes 633 of the firm s… recall
FDA
· Integra LifeSciences Corp. (NeuroSciences) · Class II
-
GSP Neonatal GALT Kit recall
FDA
· Wallac Oy · Class II
-
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component recall
FDA
· W L Gore & Associates, Inc. · Class II
-
Solar GI System (Water Perfusion) recall
FDA
· Laborie Medical Technologies Corp · Class II
-
4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A… recall
FDA
· Bard Access Systems, Inc. · Class II
-
CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
FDA
· Bard Access Systems, Inc. · Class II
-
1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935… recall
FDA
· Bard Access Systems, Inc. · Class II
-
7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
FDA
· Bard Access Systems, Inc. · Class II
-
CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
FDA
· Bard Access Systems, Inc. · Class II
-
CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
FDA
· Bard Access Systems, Inc. · Class II
-
CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
FDA
· Bard Access Systems, Inc. · Class II
-
5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12… recall
FDA
· Bard Access Systems, Inc. · Class II
-
5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr… recall
FDA
· Bard Access Systems, Inc. · Class II
-
1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110… recall
FDA
· Bard Access Systems, Inc. · Class II
-
CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code:… recall
FDA
· Bard Access Systems, Inc. · Class II
-
5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen… recall
FDA
· Bard Access Systems, Inc. · Class II
-
CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
FDA
· Bard Access Systems, Inc. · Class II
-
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748… recall
FDA
· Bard Access Systems, Inc. · Class II
-
Covidien Shiley Disposable Decannulation Plug recall
FDA
· Covidien, LP · Class II
-
Zeiss Intrabeam Spherical Applicator 1.5 cm recall
FDA
· Carl Zeiss Meditec AG · Class II
-
IntelliCuff, Portable automatic cuff pressure controller recall
FDA
· Hamilton Medical AG · Class II
-
Medtronic Harmony Delivery Catheter System recall
FDA
· Medtronic Heart Valves Division · Class I
-
Breathing circuit set, coaxial recall
FDA
· Hamilton Medical AG · Class I
-
MorningStar Farms Hot & Spicy Sausage Patties… recall
FDA
· Mars Snacking · Class II
-
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan… recall
FDA
· Mars Snacking · Class II
-
Pearl Milling Company Original Pancake & Waffle Mix Complete (Mezcla Para… recall
FDA
· Cereles En General Sas · Class I
-
Splashwire Hydrophilic Guide Wire recall
FDA
· Merit Medical Systems, Inc. · Class II
-
STAAR ICL Calculation Software Software Version: Version 8.00 Product… recall
FDA
· Staar Surgical AG · Class II
-
Mito Red Light, Super Mobile recall
FDA
· Mito Red Light Inc · Class II
-
Medtronic O-arm O2 Imaging System recall
FDA
· Medtronic Navigation, Inc.-Boxborough · Class II
-
REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A… recall
FDA
· Arrow International, LLC · Class I
-
REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20… recall
FDA
· Arrow International, LLC · Class I
-
REF: PICC ACCESS TRAY/ASK-04001-CG1 recall
FDA
· Arrow International, LLC · Class I
-
REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A… recall
FDA
· Arrow International, LLC · Class I
-
REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP; PSI KIT: 8.5 FR X 4 1/8 IN (10… recall
FDA
· Arrow International, LLC · Class I
-
REF: ACCESS TRAY/ASK-04001-MC3 recall
FDA
· Arrow International, LLC · Class I
-
REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC… recall
FDA
· Arrow International, LLC · Class I
-
REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B… recall
FDA
· Arrow International, LLC · Class I
-
REF: SPINAL ANESTHESIA KIT/ASA-24090-SB; SPINAL ANESTHESIA… recall
FDA
· Arrow International, LLC · Class I
-
REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F… recall
FDA
· Arrow International, LLC · Class I