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-2412-2014
  • 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=129306
  • 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
    Eye tray - Product Code OJK
  • 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 900-1780, 25 lots: 112010094 112020415 112041205 112051885 112072786 112083376 112083453 112104301 112114612 112125037 113015436 113036758 113057839 113068042 113078279 113088764 113099281 113109757 131110203 131110602 140111178 140211654 140312436 140513114 140513454
  • Product Classification
    Ophthalmic 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
    OPHTALMIC PACK - || (1) GOWN LGE SMS NON REINF TIWRAP || (1) IODINE POVIDONE 1oz. || (2) TOWEL ABSORBENT 15" x 20" UF || (1) SYRINGE 3cc W/NEEDLE 21 G X 1 Y. UF || (6) COTION TIP APPLICATOR 6" WOOD || (1) TABLE COVER REINFORCED 50" X 90" UF || (1) PAD EYE 2 1/8 X 2 5/8 || (1) CYSTOTOMO IRRIG. PEARCE 25G X 5/8 || (1) SHIELD EYE UNIVERSAL || (1) Pr. GLOVES SURG.# 7% LATEX || (10) SPONGE EYE SPEAR MICRO || (1) SYRINGE 1cc TUBER. 25G X 5/8 SITIP UF || (10) GAUZE SPONGES 4" X 4" 12PL Y || (1) Pr. GLOVES SURG. 8 POWDER LATEX || (1) MAYO STAND COVER REINFORCED UF || (1) BLADE 15D WITH HANDLE (STABKNIFE) || (1) EYE DRAPE || (1) GOWN LARGE STANDARD SMS || (1) TRAY 3/COMPART || (1) BAG ZIP LOCK || (1) ANGLED FULL HANDLE || (1 ) Pr. GLOVES SURGICAL# 6% LATEX || 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