Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Accurus 2500 Standalone Vitreous Probe REF 8065741018 Recalled by Alcon Research, Ltd. Due to Insufficient seal on the outside packaging, potentially affecting...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Alcon Research, Ltd. directly.
Affected Products
Accurus 2500 Standalone Vitreous Probe REF 8065741018; Accurus 23 GA Standalone Vitreous Probe REF 8065750821; Accurus 25+ 2500 CPM Standalone Vitreous Probe REF 8065751122; Anterior Accurus Probe with Infusion Needle REF 8065803650; Single Use Sterile Probes Rx only. Intended to provide the surgeon with a single-use probe for performing vitrectomy surgical procedures while using the Alcon Accurus vitrectomy console.
Quantity: 35,475 units
Why Was This Recalled?
Insufficient seal on the outside packaging, potentially affecting the sterility of the product.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Alcon Research, Ltd.
Alcon Research, Ltd. has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report