Events

Recall of MicroSTAAR Injector, MSI-PF

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Staar Surgical Co 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
    28896
  • Event Risk Class
    Class 3
  • Event Number
    Z-0957-04
  • Event Initiated Date
    2004-04-21
  • Event Date Posted
    2004-07-20
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2012-07-26
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=32722
  • 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
    Lens, Guide, Intraocular - Product Code KYB
  • Reason
    Cracking of the distal end of the injector occurs during locking of the cartridge into the nose cone of the injector.
  • Action
    Recall will be implemented by visits by company representatives.

Device

MicroSTAAR Injector, MSI-PF
  • Model / Serial
    Lot 1186591 Expires 12/31/06 Lot 1186692 Expires 12/31/06
  • Product Classification
    Ophthalmic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    MicroSTAAR Injector, MSI-PF || Packed ten per box.
  • Manufacturer
    Staar Surgical Co Inc

Manufacturer

Staar Surgical Co Inc
  • Manufacturer Address
    Staar Surgical Co Inc, 1911 Walker Ave, Monrovia CA 91016-4846
  • Source
    USFDA