-
Medline procedure kits labeled as: 1) ANGIO DRAPE PACK (DRLUL)-LF… recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits labeled as: 1) ANGIO PACK, Pack Number DYNJ50624A recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits labeled as: 1) BILATERAL FACET TRAY… recall
FDA
· Medline Industries, LP · Class II
-
Prelude IDEAL 4 F Hydrophilic Sheath Introducer recall
FDA
· Merit Medical Systems, Inc. · Class II
-
NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer… recall
FDA
· Zimmer, Inc. · Class II
-
Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal… recall
FDA
· Orthofix U.S. LLC · Class II
-
namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW recall
FDA
· Medline Industries, LP · Class II
-
namic convenience kits labeled as: MTS,COLOR,PML,KIT,-,FRENCH HOSPITAL PG recall
FDA
· Medline Industries, LP · Class II
-
namic convenience kits labeled as: KIT,ARTERIAL,60,(152CM),PG recall
FDA
· Medline Industries, LP · Class II
-
namic convenience kits labeled as: PML,72,ADULT,FLL-MLL,-,OEM recall
FDA
· Medline Industries, LP · Class II
-
CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital… recall
FDA
· St. Jude Medical · Class II
-
Banner University Med Ctr recall
FDA
· American Contract Systems Inc · Class II
-
Banner Health Systems Product Name: Lap Pack - 170307 Model recall
FDA
· American Contract Systems Inc · Class II
-
Banner Health Systems Product Name: Cysto Pack Model recall
FDA
· American Contract Systems Inc · Class II
-
Baxter NovumIQ Syringe INFUSION SYSTEM recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500, Product Code 4091000 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Floor mounting column TS 7500 U, Product Code 1730732 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Stationary column TruSystem 7500 U, Product Code 1730731 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Mobile column TruSystem 7500 U, Product Code 1730720 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Mobile column TruSystem 7500, Product Code 1717023 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Floor mounting column TruSystem 7500, Product Code 1717021 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Stationary column TruSystem 7500, Product Code 1717020 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Operating table column TS7500 MOBIUS, Product Code 1704695 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Premier Solo Diamond - Large Invented Cone recall
FDA
· Premier Dental Products Co · Class II
-
Synapse PACS Software Version 7.4.x recall
FDA
· FUJIFILM Healthcare Americas Corporation · Class II
-
CRANI PACK, Model recall
FDA
· American Contract Systems Inc · Class II
-
CAPNOCHECK BCI Airway Adapter recall
FDA
· Smiths Medical ASD, Inc. · Class II
-
CAPNOCHECK BCI Airway Adapter recall
FDA
· Smiths Medical ASD, Inc. · Class II
-
Comprehensive Shoulder Stem, Comprehensive Micro Stem… recall
FDA
· Zimmer Orthopedics Manfacturing Limited-Galway · Class II
-
Merge Cardio, Model recall
FDA
· Merge Healthcare, Inc. · Class II
-
VERICIS, Merge Cardio, Model recall
FDA
· Merge Healthcare, Inc. · Class II
-
VERICIS, Merge Cardio, Model recall
FDA
· Merge Healthcare, Inc. · Class II
-
VERICIS, Merge Cardio, Model recall
FDA
· Merge Healthcare, Inc. · Class II
-
VERICIS, Merge Cardio, Model recall
FDA
· Merge Healthcare, Inc. · Class II
-
Introcan Safety 3 Closed IV Catheter 22 Ga recall
FDA
· B Braun Medical Inc · Class II
-
Zebra Thermal Barcode Printer GX430t, Model no recall
FDA
· Remel, Inc · Class II
-
Medline procedure kits labeled as: 1) EYE PACK, Pack Number VAL038BSCLC recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098 recall
FDA
· Medline Industries, LP · Class II
-
Origin Data Management software versions 3.1.0, 3.1.1, 3.1.2, 3.2.0, 3.2.1 recall
FDA
· Brainlab AG · Class II
-
IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit recall
FDA
· Angiodynamics, Inc. · Class II
-
Candida ID Antigen, REAG, AG recall
FDA
· Immuno-Mycologics, Inc · Class II
-
DxI 9000 Access Immunoassay Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
DxI 9000 Access Immunoassay Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
Access 2 Immunoassay Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II
-
Microstream Instructions for Use and Part Number used with - Product… recall
FDA
· Oridion Medical 1987 Ltd. · Class II