Reported Mar 27, 2024 · Ongoing
Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: D.O.R.C. Dutch Opthalmic Research Center Intl B.V. · Scheijdelveweg 2 · Zuidland · N/A
Is this the product you have?
- Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)
- Lot codes and dates
- Product Number7223.ALC
- UDI/DI08717872014173; All lots starting with a number between 2470 and 18705
- Amount recalled
- 14 boxes x 6 units per box = 84 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new D.O.R.C. Dutch Opthalmic Research Center Intl… recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.