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-2509-2014
  • 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=129542
  • 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
    Orthopedic tray - Product Code OJH
  • 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
    Code 900-2903, 4 lots 113026303 113057705 113068034 113088858
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • 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
    ORTHOPEDIC IMPLANT || PACK CUSTOMED USA, CODE 900-2903 || CONTENTS: || (1) CAUTERY TIP POLISHER UF || (1) SKIN MARKER W/RULER || (1) BAG SUTURE FLORAL || (1) U - DRAPE 60" X 70" WITAPE SPLIT 6" X 21" || (1) TUBE SUCTION CONNECT W' X 12' UF || (2) PAD ABDOMINAL 8" X 7.5" || (1) BAG GLASSINE || (1) YANKAUER SUCTION TUBE W/0 VENT LIF || (2) LITE GLOVE UF || (1) SOLUTION SURGICAL DURAPREP 26ML LIF || (2) TABLE COVER REINFORCED 50" X 90" LIF || (1) BLADE SURGICAL# 10 STAINLESS STEEL || (1) MAYO STAND COVER REINFORCED LIF || (1) SHEET SPLIT W/ADHES 108" X 77" STD SMS L/F || (5) TOWELS ABSORBENT 15" X 20" UF || (1) STOKINETIE IMPERVIOUS 14" X 48" LIF || (2) DRAPE SHEET 70" X 100" LIF || (1) *GLOVE# 7'!h SURGEON NEUTRALON LATEX || (5) LAP SPONGE PREWASH 18" X 18" XRD LIF || (1) *GLOVE # 8 SURGEON NEUTRALON LATEX || (1) SKIN STAPLE 35 WIDE UF || (1) *GLOVE# 8'!h SURGEON NEUTRALON LATEX || (1) TRAY MAYO LGE || (1) GOWN SURG REINFORCED XL TOWEUWRAP || (1) DRAPE TOP W/ADHES 108" X 50" STD SMS UF || (2) GOWN XL SMS IMPERVIOUS REINFORCED UF || (1) BULB SYRINGE 60cc CLEAR || (1) CAUTERY PENCYL ROCKER SWITCH UF || (1) UTILITY BOWL 16oz LIF || (1) BLADE SURGICAL# 20 STAINLESS STEEL || (1) UTILITY BOWL QUART 32oz LIF || (4) DRAPE UTILITY WITAPE UF || (1) DRAPE INCISION 23" X 17" UF || Product Usage: || 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