FDA Medical Device Recalls (openFDA)
Barco N.V.: Optional MDRC-1119 Front Cover Attachment Kit for review display monitors. Product Usage: The product is an optional kit, intended to be attached in front of the LCD panel of a review display (MDRC-1119).
- Recall number
- Z-0527-2019
- Recalling firm
- Barco N.V.
- Product
- Optional MDRC-1119 Front Cover Attachment Kit for review display monitors. Product Usage: The product is an optional kit, intended to be attached in front of the LCD panel of a review display (MDRC-1119).
- Status
- Terminated
- Initiated
- 2017-03-30
- Posted
- not on file
- Terminated
- 2020-05-04
- Reason
- If metal strips are removed and re-applied to another display, there is potential for the metal strips to be deformed resulting in a smaller contact surface with the front cover magnet strips. There is a risk that the protective front cover could come loose and may fall down.
- Root cause
- Device Design
- Action
- Customers were notified via email on about 03/30/2017. Customers were alerted that a safety related update has been made to the installation manual. A safety notice has been shipped to distributors with the updated installation instructions manual and an acknowledgement letter. Distributors were asked to do the following: a) Inform all your customers who have purchased the Front Cover Kit by sending them the Safety Notice; b) Send the updated installation instructions to all your customers who have purchased the Front Cover Kit; c) Fill out the acknowledgment letter; attach and send in reply to this email.
- Quantity
- 2,087 units
- Distribution
- Worldwide - US Nationwide Distribution to CA, IL, GA, TX, and WI. In the countries of Belgium, Brazil, Canada, Czech Republic, Denmark, Finland, France, Germany, Italy, Japan, Poland, Saudi Arabia, South Africa, South Korea, Spain, Sweden, Taiwan, Turkey.
- Lot, serial or model codes
- Part Numbers C9826108, C9826109, C9826096, C9826097
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- OWB
- Firm FEI
- 3004455125
- Firm city
- Kortrijk
- Firm state
- not on file
- Firm country
- Belgium
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28