TDC VELOCE 23G Cutter Recall Issued by D.O.R.C.
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. is recalling TDC VELOCE 23G Two Dimensional Cutter devices due to reports of loose outer knives.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 28, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-device.
What Happened D.O.R.C. Dutch Opthalmic Research Center Intl B.V. initiated a recall of TDC VELOCE 23G Two Dimensional Cutter devices after receiving complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Which Products Are Affected The recall covers "TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM with article numbers 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00. A total of 314 boxes (1884 units) are affected. Specific UDI-DI and lot numbers are listed in the recall. Distribution was US Nationwide and to 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, and Turkey. The recall number is Z-2322-2026.
What You Should Do Consumers should follow instructions provided in the firm's notification letter regarding the recalled devices.
Why This Matters The Class II recall addresses a defect that could lead to device malfunction during use.
Source FDA recall number Z-2322-2026, report date 20260617.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,196 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 28, 2026.
Frequently Asked Questions
Common questions about this FDA recall.