Events

Recall of Device Recall Customed

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Customed, Inc.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    68536
  • Event Risk Class
    Class 1
  • Event Number
    Z-2323-2014
  • Event Initiated Date
    2014-05-20
  • Event Date Posted
    2014-08-29
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2017-08-14
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=129161
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    laparoscopy kit - Product Code FDE
  • Reason
    Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). this could result in an injury to the patient due to product contamination or loss of sterility condition.
  • Action
    Customed Inc. sent a Recall Notification letter dated June 3, 2014 via email and followed by letter to all affected customers. The letter identified the affected products, problem and actions to be taken. The letter informed customers if the affected products are in their inventory to: 1. Remove products from sale (quarantine them) and cease distribution. 2. Complete and return the enclosed acknowledgement form to Customed Inc .Recall Coordinator. Affected products should be returned to Customed Inc for credit. Customers with questions were instructed to contact Customed Inc. Recall Coordinator at 1-787-801-0100 Ext. 7540

Device

Device Recall Customed
  • Model / Serial
    Product code 900-414, 26 lots: 112030868 112041328 112051656 112062284 112072802 112093940 112104108 112114600 113015696 113025963 113036361 113036800 113057485 113068047 113068170 113088863 113089072 113099574 131110261 131210813 140111100 140211669 140311938 140412466 140412887 140513363
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.
  • Product Description
    LAPAROSCOPY CHOLE PACK - - || ( 1) STRIP STERI CLOSURE W' X 4" LIF || ( 1) TABLE COVER REINFORCED 50" X 90" LIF || ( 1) DRAPE LAP ABDOMINAL W/POUCH 102" X 122" X 78" LIF || (2) GOWN LGE SMS IMPERVIOUS REINFORCED LIF || ( 1) GOWN XL SMS IMPERVIOUS REINFORCED L/F || (5) TOWELS ABSORBENT 15" X 20" LIF || (5) LAP SPONGE PREWASH 18" X 18" XRD LIF || (4) DRAPE UTILITY WIT APE LIF || ( 1) COVER CAMERA W/ELAST LIF || (2) GAUZE SPONGE 4" X 4" 12PL Y LIF || ( 1) NEEDLE ULTRA VERES 120mm LIF || (2) DRAPE SHEET 41 " X 58" SMS LIF || ( 1) SCALPEL WEIGHTED SAFETY #11 || ( 1) TUBING INSUFFLATING OPEN TIP W/0 VENT LIF || ( 1) DRESSING TEGADERM 4" X 4 %" LIF || ( 1) TUBE SUCTION CONNECT X" X 12' LIF || ( 1) MAYO STAND COVER REINFORCED LIF || ( 1) SUTURE BAG FLORAL LIF || ( 1) Pk. STERI STRIP LAP SET LATEX || ( 1) CORD LAPAROSCOPY MONOPOLAR LIF || ( 1) MAYO TRAY SMALL LIF || ( 1) TIME OUT BEACON NON WOVEN ST. LIF || (1) SKIN MARKER INK W/8 LABEL TIME OUT/RULER LIF || ( 1) BAG ZIP LOCK PLASTIC 6" X 10" || EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents
  • Manufacturer
    Customed, Inc

Manufacturer

Customed, Inc
  • Manufacturer Address
    Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
  • Manufacturer Parent Company (2017)
    Customed Inc
  • Source
    USFDA