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-2368-2014
  • 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=129262
  • 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
    Accessories, operating-room, table (kit) - Product Code FWZ
  • 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 900-1042, 12 lots: 113026163 113036737 113046994 113057378 113078232 113078669 113089153 113109704 131110065 131110610 140111137 140312045
  • Product Classification
    General and Plastic Surgery 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
    ARTHROSCOPY PACK - || (1) SURGICAL DURAPREP SOLUTION 26ML LIF || (1) ESMARK BANDAGE || (1 ) ELASTIC BANDAGE 6" X 5yds LIF || (1) NEEDLE & BLADE COUNTER 20C FOAM/MAG || (1) TUBE SUCTION CONNECTING W X 12' LIF || (1) SHEET EXTREMITY ABS. 125" X 85" SMS || (1) DRAPE LASER CAMERA W/EL || (3) TOWELS ABSORBENT 15" X 20" LIF || (2) CONTAINER SPECIMEN 4oz. WITH LID & LABEL || (1) BABY BLANKET IMP. POLY ABS. LIF || (1) NEEDLE HYPODERMIC 20G X 1%'' || (10) GAUZE SPONGES 4" X 4" 16PLY || (1) BLADE SURGICAL #11 CARBON STEEL || (1) TABLE COVER REINFORCED 50" X 90" LIF || (1) IMPERVIOUS STOCKINETTE || (1) SHEET DRAPE 42" X 55" LIF || (1) SUTURE BAG FLORAL LIF || (1) U-DRAPE 60" X 70" WITH TAPE SPLIT || (1) MAYO STAND COVER REINFORCED LIF || (2) GOWN IMPERVIOUS REINFORCED SMS LARGE || (4) STRIPS TAPE || (1) SYRINGE 20cc WITHOUT NEEDLE LUER LOCK LIF || (1) GAUZE KERLIX 4.5 X 4.1 YO 6PL Y || (1) GOWN IMPERVIOUS EXTRA REINFORCED X-LARGE TOWEL & WRAP || 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