-
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety… recall
FDA
· ICU Medical, Inc. · Class II
-
Contour Product Name: Contour Gold Eyelid Weight Model recall
FDA
· Meddev Corp · Class II
-
Contour Product Name: Contour Gold Eyelid Weight Model recall
FDA
· Meddev Corp · Class II
-
MedicaLyte Liquid Bicarbonate Concentrate recall
FDA
· Nipro Renal Soultions USA, Corporation · Class I
-
H&C Farms Raw Premium Tomatoes, Naturally Grown from Seed Net WT 25 Lbs… recall
FDA
· Hanshaw & Capling Farms, LLC · Class I
-
Introducer Kit- Tearaway MicroSlide recall
FDA
· Galt Medical Corporation · Class II
-
Introducer Needle recall
FDA
· Galt Medical Corporation · Class II
-
Introducer Kit- Coaxial Dilator recall
FDA
· Galt Medical Corporation · Class II
-
GALT Guidewire recall
FDA
· Galt Medical Corporation · Class II
-
B Braun Interventional ELITE HV Hemostasis Valve Introducer System recall
FDA
· Galt Medical Corporation · Class II
-
B Braun Interventional Coaxial Dilator recall
FDA
· Galt Medical Corporation · Class II
-
GALT Centeze Catheter recall
FDA
· Galt Medical Corporation · Class II
-
Philips Tempus Pro Patient Monitor recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II
-
Artix MT Thrombectomy Device recall
FDA
· Inari Medical - Oak Canyon · Class II
-
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set recall
FDA
· Ambu · Class II
-
Clindamycin HCl Capsule, 300 mg, QTY: 30 Capsules per bottle, Rx Only… recall
FDA
· RemedyRepack Inc. · Class II
-
Enhanced Verify Evaluation Handset (CFN HH90130FA) recall
FDA
· Medtronic Neuromodulation · Class II
-
myQA iON recall
FDA
· IBA Dosimetry GmbH · Class II
-
Tibial Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
L-Shaped Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Posterior Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Distal Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Quantum Informatics - VISION / LIVE VUE Product Name: Monitor… recall
FDA
· Spectrum Medical Ltd. · Class II
-
Quantum Informatics - VIPER Product Name: Monitor, Physiological… recall
FDA
· Spectrum Medical Ltd. · Class II
-
HistoCore PELORIS 3, Model recall
FDA
· Leica Biosystems Melbourne Pty Ltd · Class II
-
3.0 Liter Disposable Set (4 sets/case) recall
FDA
· Belmont Instrument LLC · Class II
-
Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled:… recall
FDA
· Dianne's Fine Desserts · Class II
-
Infuvite Adult, multiple vitamins injection, Baxter… recall
FDA
· Mckesson Medical-Surgical Inc. Corporate Office · Class II
-
Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL… recall
FDA
· Mckesson Medical-Surgical Inc. Corporate Office · Class II
-
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP… recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II
-
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount recall
FDA
· Ihb Operations B.V. · Class II
-
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090… recall
FDA
· Radiometer Medical ApS · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
InPen smart insulin pen recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Merit Medical recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical recall
FDA
· Merit Medical Systems, Inc. · Class II
-
BD PYXIS MEDBANK (Name recall
FDA
· CareFusion 303, Inc. · Class II
-
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 recall
FDA
· Medtronic Xomed, Inc. · Class II
-
Apple Juice recall
FDA
· S Martinelli & Company · Class II
-
Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION… recall
FDA
· Channel Medsystems, Inc. · Class II
-
Maquet VH-3010 Power Supply recall
FDA
· Maquet Cardiovascular, LLC · Class II
-
HeartMate Mobile Power Unit recall
FDA
· Thoratec LLC · Class I
-
restor3d Cordera Hip System recall
FDA
· Conformis Inc. · Class II
-
Aveir DR Leadless Pacemaker (LP) Ventricular Device recall
FDA
· Abbott Medical · Class II
-
Philips DXR System, DuraDiagnost Rel recall
FDA
· Philips North America Llc · Class II
-
Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System recall
FDA
· Philips North America Llc · Class II
-
MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0… recall
FDA
· CareFusion 303, Inc. · Class II
-
AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform… recall
FDA
· ZOLL Circulation, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I