Recall Record

Zuidland, Netherlands

D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls

2 recalls recorded since 2018, most recently on 30 April 2026. 2 are listed as ongoing. Status and classification are as published by the FDA.

Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0

Ongoing Class II Medical devices

Recall started
30 April 2026
Reason
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Distribution
Worldwide - US Nationwide and the countries of AUSTRALIA, AUSTRIA, BELGIUM, BULGARIA, CZECHIA, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, HONG KONG, IRELAND, ITALY, JAPAN, NETHERLANDS, NEW ZEALAND, POLAND, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, TAIWAN, TURKEY.
Initiated
Voluntary: Firm initiated
Recall numbers
Z-2322-2026, Z-2324-2026, Z-2323-2026

Ongoing Class II Medical devices

Recall started
15 January 2024
Reason
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.
Distribution
US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.
Initiated
Voluntary: Firm initiated
Recall numbers
Z-1333-2024, Z-1332-2024, Z-1331-2024

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.