D.O.R.C. Dutch Opthalmic Research Center Intl B.V. 2024-03-27 Health serious FDA
Health · FDA · Recall #FDA-Z-1333-2024
Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm) Recall
Issued March 27, 2024 · D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
In March 2024, D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalled the Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm), a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.
What you should do
- 1 Stop using Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm) right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact D.O.R.C. Dutch Opthalmic Research Center Intl B.V. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
- Category
- Health
- Recall date
- March 27, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.
- Recall number
- FDA-Z-1333-2024
- Made in
- Netherlands
- Issuing agency
- FDA
In context
- D.O.R.C. Dutch Opthalmic Research Center Intl B.V. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.