echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > State Food and Drug Administration: Medical devices such as Kangwei De, Bonmei Orthopedics, Edwards are being recalled

    State Food and Drug Administration: Medical devices such as Kangwei De, Bonmei Orthopedics, Edwards are being recalled

    • Last Update: 2022-02-20
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    On January 20, the State Food and Drug Administration issued an announcement informing that four companies including Convid and Edward have voluntarily recalled some of their illegal products
    .
    These include foam dressings, valvuloplasty rings, and more
    .
    The details are as follows: Edwards Lifesciences LLC voluntarily recalled the valvuloplasty ring Tricuspid Annuloplasty Ring Edwards (Shanghai) Medical Supplies Co.
    , Ltd.
    reported that due to a specific model and a specific batch of products, there was an error in the expiration date on the product label, the manufacturer Edwards Lifesciences LLC voluntarily recalled the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration No.
    : National Machinery Injection 20173466532)
    .
    The recall level is three
    .
    ConvaTec Inc.
    has voluntarily recalled the foam dressing AQUACEL™ Foam Hydrofiber™ Dressing.
    ConvaTec Inc.
    has voluntarily recalled the foam dressing AQUACEL™ Foam Hydrofiber™ Dressing (Registration No.
    : National Machinery Injection 20173640956)
    .
    The recall level is three
    .
    Biomet Orthopedics reported that Zimmer (Shanghai) Medical International Trading Co.
    , Ltd.
    voluntarily recalled the revision femoral stem and accessories Arcos Modular Revision System and shoulder joint system Comprehensive Shoulder System.
    Due to the specific model and specific batch of products, there is a Porous plasma spray coating (PPS) has been wrongly reworked.
    20163461304, State Machinery injected 20153463900) voluntarily recalled
    .
    The recall level is two
    .
    MAILLEFER INSTRUMENTS HOLDING SARL MAILLEFER INSTRUMENTS HOLDING SARL Dentsply Sirona Dental Products (Shanghai) Co.
    , Ltd.
    has voluntarily recalled mechanical root canal files and dental files.
    Dental Instruments Holding Company voluntarily recalled mechanical root canal files and dental files (registration certificate number: National Machinery Injection 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029)
    .
    The recall level is three
    .
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.