Recall of Device Recall Stylus Brand Angled Knives

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Surgical Specialties Puerto Rico, 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
    28948
  • Event Risk Class
    Class 2
  • Event Number
    Z-0945-04
  • Event Initiated Date
    2004-03-03
  • Event Date Posted
    2004-07-20
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2004-09-10
  • Event Source
    USFDA
  • Event Source URL
  • 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
    Knife, Ophthalmic - Product Code HNN
  • Reason
    Incorrect placement of the blade in the foam of product results in blade poking through packaging. compromised sterility and injury to healthcare worker.
  • Action
    Customers were notified by e-mail and fax of the recall during the period of March 3, 2004 to April 1, 2004. Customers were requested to return the product to Surgical Specialties Corporation, Reading, PA 19606.

Device

  • Model / Serial
    Model No. Lot # Exp. date 52-2835 M454660 2/2009 52-2835 M317210 7/2008
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Distribution was nationwide and internationally
  • Product Description
    Stylus Angled Knife - 52-2835 Clear Corneal Knife, double bevel, parallel sides, angled, full handle, 2.85mm
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Surgical Specialties Puerto Rico, Inc., Road 115 Km.12.9, Rincon PR 00677
  • Source
    USFDA