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    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG (Introducer Catheter), REF: FCL-069-00/A FCL-069-02/A FCL-069-03/A For the introduction of various types of pacing or defibrillator leads and catheters.

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DYB·June 11, 2024

    Thomas Medical Products, SafeSheath Long, (Tear-Away Sheath Introducer Set with Integral Hemostasis Valve) for use during vascular interventional procedures. Part No. FCL-051-00, Catalog No. HLS2507MCN; and Part No. FCL-051-02, Catalog No. HLS2507MCN.

    FDA Recall
    Terminated ·Thomas Medical Products Inc·Product code DYB·December 16, 2010

    Thomas Medical Products, Safesheath MSP Introducer Sheath Kit with Integral Hemostasis Valve for use during vascular interventional procedures. SafeSheath Sealing Adapter, Part No. FCL-094-03, Catalog No. SSSA-EW-09; SafeSheath Sealing Adapter, Part No. FCL-141-01, Catalog No. 369826; Transvalvular Insertion Tool (TVI), Part #MIS-099-00, Catalog No. TVI-07; Transvalvular Insertion Tool (TVI), Part #MIS-122-00, Catalog No. TVI-09; and CPS SafeSheath Sealing Adapter, Part No. XD-2754-00, Catalog No. 410195.

    FDA Recall
    Terminated ·Thomas Medical Products Inc·Product code DYB·December 16, 2010

    16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DYB·February 13, 2026

    Focal Sim radiation therapy treatment planning system

    FDA Recall
    Terminated ·Elekta, Inc.·Product code MUJ·December 19, 2014

    STERIS 4085, 5085 & 5085SRT Surgical Tables

    FDA Recall
    Terminated ·Steris Corporation·Product code FQO·May 14, 2010

    Boston Scientific mach 1 Guide Catheter, 8F, FCL 3.5 SH Femoral Curve Left 3.5, REF 34358-268, UPN H749343582680, Sterile EO Made in Mexico Avenida Norske Edicficio G1, Local B y H Parque Industrial La Mesa, Fracc. Rubio La Mesa, Tijuana, B.C. Mexico C.P. 22550

    FDA Recall
    Terminated ·Boston Scientific·Product code DQY·September 11, 2007

    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG/Worley advanced CSG (Introducer Catheter kit), REF: FCL-083-02/A WOR-CSG-B1-09/A WOR-CSG-B2-09/A WOR-CSG-BL1-09/A WOR-CSG-E-90/A For the introduction of various types of pacing or defibrillator leads and catheters.

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DYB·June 11, 2024

    FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    Transluminal Biliary Biopsy Forceps Set Forceps, Biopsy, Non-Electric Intended for access to and biopsy of tissue within the biliary ductal system

    FDA Recall
    Terminated ·Cook Inc.·Product code FCL·April 15, 2016

    FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.051

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps UPN/Catalog Number: MOO513330 The Radial Jaw 4 Large Capacity Inner Pouch, 240cm UPN M00513330 is a single unit which is packaged into a Box of 20 units (UPN M00513331), and a Box of 80 units (UPN M00513334). Single packaged units of M00513330 are not sold individually.

    FDA Recall
    Terminated ·Boston Scientific Corporation·Product code FCL·May 6, 2010

    Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps Box 80, 240cm UPN/Catalog Number: M00513334

    FDA Recall
    Terminated ·Boston Scientific Corporation·Product code FCL·May 6, 2010

    Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps Inner Pouch 240cm, Box 20 UPN/Catalog Number: M00513331

    FDA Recall
    Terminated ·Boston Scientific Corporation·Product code FCL·May 6, 2010

    Medtronic REF: MMT-7008B, Enlite Glucose Sensor for the following packaging: ENLITE PLUS 23L 1CL / GTIN: 00643169541719 ENLITE PLUS 2L 1CL PR/ GTIN: 00643169786738 ENLITE PLUS 1PK 23L 1CL/ GTIN: 00763000421304 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes.

    FDA Recall
    Open, Classified ·Medtronic Inc.·Product code MDS·February 26, 2021

    Medtronic, REF: MMT-7008A, Enlite Glucose Sensor for the following packaging: ENLITE PLUS 5PK 23L 1CL /GTIN: 20643169541706, ENLT PLUS 5PK 2L 1CL PR/ GTIN: 20643169786725, ENLITE PLUS 5PK 23L 1CL/ GTIN: 20763000421292 - Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes.

    FDA Recall
    Open, Classified ·Medtronic Inc.·Product code MDS·February 26, 2021

    NEONATE 3 DISPOSABLE BLOOD PRESSURE CUFF WITH 2 TUBES, a disposable 1 piece cuff for single patient use only. Sold under the Welch Allyn ''Tycos'' label with Part # 5082-103-2, 5082-102-2CL , and sold as part of a multi-pack (1 of each size) with Part #5082-241-10 - Welch Allyn Inc., Skaneateles Falls, NY; Allegiance Healthcare ''Tactics'' label with Part # 30502-112 and 30502-212 - Allegiance Healthcare Corp., McGaw Park, IL; and Arden label with Part # 5084-103-2, and 635-5084-103-2 - Arden, Skaneateles, NY.

    FDA Recall
    Terminated ·Welch Allyn Inc·Product code DXQ·March 1, 2004

    NEONATE 4 DISPOSABLE BLOOD PRESSURE CUFF WITH 2 TUBES, a disposable 1 piece cuff for single patient use only. Sold under the Welch Allyn ''Tycos'' label with Part # 5082-104-2, 5082-104-2CL, and sold as part of a multi-pack (1 of each size) with Part #5082-241-10 - Welch Allyn Inc., Skaneateles Falls, NY; Allegiance Healthcare ''Tactics'' label with Part # 30502-113 and 30502-213 - Allegiance Healthcare Corp., McGaw Park, IL; and Arden label with Part # 5084-104-2 and 636-5084-104-2 - Arden, Skaneateles, NY.

    FDA Recall
    Terminated ·Welch Allyn Inc·Product code DXQ·March 1, 2004