-
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
-
CVAC Aspiration System recall
FDA
· Calyxo, Inc. · Class I
-
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable… recall
FDA
· Covidien, LP · Class I
-
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
-
BD Pyxis: Anesthesia Station ES recall
FDA
· CareFusion 303, Inc. · Class II
-
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm… recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm… recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm… recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus… recall
FDA
· Microbiologics Inc · Class II
-
Proxima Drape labeled as ORTHO TRAUMA CDS, TOTAL KNEE AUX PACK… recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P… recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as HEAD AND NECK OSIS, WILLIS SHOULDER PACK… recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as FACE LIFT. Sterile surgical drape recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape recall
FDA
· Medline Industries, LP · Class II