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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94022

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
January 15, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)

Z-1331-2024
Recall number
Z-1331-2024
Initiated
January 15, 2024
Classification
Class II
Status
Ongoing
Quantity
14 boxes x 6 units per box = 84 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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.

Code information

Product Number: 7223.ALC; UDI/DI: 08717872014173; All lots starting with a number between 2470 and 18705.

Distribution pattern

US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.

device · product 2 of 3

Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)

Z-1332-2024
Recall number
Z-1332-2024
Initiated
January 15, 2024
Classification
Class II
Status
Ongoing
Quantity
21 boxes x 6 units each = 126 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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.

Code information

Product Number: 7225.ALC; UDI/DI: 08717872014203; All lots starting with a number between 2470 and 18705.

Distribution pattern

US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.

device · product 3 of 3

Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)

Z-1333-2024
Recall number
Z-1333-2024
Initiated
January 15, 2024
Classification
Class II
Status
Ongoing
Quantity
13 boxes x 6 units per box = 78 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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.

Code information

Product Number: 7227.ALC; UDI/DI: 08717872031897; All lots starting with a number between 2470 and 18705.

Distribution pattern

US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.