BEUDAMED
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    Drill bits used in ENDOTINE Forehead 3.5 and 3.0, Catalog Number: CFD-010-4203 and CFD-010-4303

    FDA Recall
    Terminated ·Coapt Systems, Inc.·Product code ---·May 23, 2003

    Endotine Transbleph 3.5 (CFD-080-0167)

    FDA Recall
    Terminated ·MicroAire Surgical Instruments, LLC·Product code HWC·May 6, 2016

    Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Sterile Co-Flex Med 4" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019

    Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging

    FDA Recall
    Terminated ·Ziehm Imaging Inc·Product code OWB·November 21, 2013

    Lasik Custom Pak containing 1 dual tip irrigator, 8 ports, 16 G, 2 packs spears, eye, ocucel, 5S, PVA, 1 cover, support, tray 2.2MIL 6FD, and 2 dressings, tegaderm, 2 3/8 x 2 3/4. All contents considered sterile unless package is opened or damaged.RX Only. Part number 10162-01. (The Vidaurri LASIK Flap Irrigators are included in the firm''s Alcon Custom Pak Part Number 10162-01 under the description of dual tip irrigator, 8 ports, 16G.)

    FDA Recall
    Terminated ·Alcon Research, Ltd·Product code LQJ·September 2, 2005

    Supreme Electrophysiology Extension Cable, REF 401984, For use with Hexapolar Catheters, Sterile EO, Rx only, St Jude Medical, 14901 DeVeau Place, Minnetonka, MN 55345. Supreme Electrophysiology Extension Cable used to connect Electrophysiology catheters to external diagnostic or therapeutic equipment. The section indexing connector located a t the distal end of the cable will only connect to SMJ Electrophysiology catheters.

    FDA Recall
    Terminated ·St. Jude Medical·Product code IKD·June 1, 2011

    St. Jude Medical Epicor UltraWand LP Handheld Ablation Device, model UW-LP-2, Sterilized with Ethylene Oxide. Single-use. The Ultra Wand LP device is designed for use with the Epicor Cardiac Ablation System. St. Jude Medical 240 Santa Ana Court, Sunnyvale, CA 94085 USA

    FDA Recall
    Terminated ·St. Jude Medical Atrial Fibrillation Division Inc·Product code OCL·June 15, 2009

    Agee-WristJack Fracture Reduction System; Item number: CFD-147. The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures. This is a single use system used for a trauma related surgery The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures. The non-perishable sterile system is packaged in an inner then outer tray and shipped in a cardboard shelf box. Orthopedic:The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures.

    FDA Recall
    Terminated ·Hand Biomechanics Lab Inc·Product code JEC·September 14, 2016

    Salivart Oral Moisturizer, packaged in 2.5 fluid ounce (73.9 mL) spray cans, Part Number: 0386-0009-75; Manufactured by Gebauer Company, Cleveland, Ohio

    FDA Recall
    Terminated ·Gebauer Company·Product code LFD·January 19, 2007

    Salvart Oral Moisturizer, 2.5 fl.oz. aerosol cans, OTC, Item Number 0386-0009-75. Distributed by: Gebauer Co., Cleveland, OH.

    FDA Recall
    Terminated ·Gebauer Co·Product code LFD·February 23, 2004

    The Zimmer Air Dermatome, REF 00- 8801- 001- 00 , Rx, non-sterile grafting instruments intended to provide variable graft thickness and width capabilities

    FDA Recall
    Terminated ·Zimmer Surgical Inc·Product code GFD·May 7, 2013

    Zimmer Air Dermatome II Width Plate, 1 in., item number 00-8851-201-00 . Width plates is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.

    FDA Recall
    Terminated ·Zimmer Surgical Inc·Product code GFD·July 4, 2016

    CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx Only Manufactured for: KCI USA, Inc. Part Number CT-H50 or CT-H25 The CelluTome Epidermal Harvesting System is intended to reproducibly cut a thin skin graft for autologous skin grafting.

    FDA Recall
    Terminated ·KCI USA, INC.·Product code GFD·November 19, 2014

    Zimmer Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimmer Air Dermatome II handpiece and width plates are packaged inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.

    FDA Recall
    Terminated ·Zimmer Surgical Inc·Product code GFD·July 4, 2016

    Zimmer Air Dermatome II Width Plate, 3 inch. Part #00-8851-203-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.

    FDA Recall
    Terminated ·Zimmer Surgical Inc·Product code GFD·July 4, 2016