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-2361-2014
  • 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=129255
  • 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 900-944, 63 lots: 110010120 110010151 110020418 110020489 110020494 110040959 110040961 110041046 110041047 110061499 110061544 110071716 110071717 110071807 110071808 110092290 110092318 110092409 110092412 110112786 110112787 110122904 110122905 111010173 111010179 111020306 111030826 111040980 111051219 111061648 111071971 111082117 111092408 111102641 111102787 111123307 112010211 112020471 112030755 112030944 112041363 112052025 112062574 112083442 112104089 112114686 113025972 113036598 113047119 113047149 113057515 113057821 113068182 113078576 113099299 113099580 131210848 131210975 140111456 140211881 140312387 140412843 140513353
  • 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
    CATARACT PACK- OJOS INC.- || (1) TABLE COVER REINF. 44" X 78" L/F || (2) MEDICINE CUP 1oz. || (2) ABSORBENT TOWEL 15" X 20" LIF || (1 0) EYE SPEAR MICRO SPONGE || (1) EYE PAD 2 1/8 X 2 5/8 LIF || (4) DRAPE UTILITY LIF || (1) EYE SHIELD UNIVERSAL || (2) GOWN LGE STANDARD SMS VELCRO/NECK || (1) MAYO STAND COVER REINF. LIF || (1) EYE DRAPE LIF || (1) SYRINGE 3cc W/0 NDL L/LOCK LIF || (1) WIPE INSTRUMENT 1MM L/F || 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