Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
25 gauge VersaVit 2.0 Vitrectomy Cutter Recalled by Synergetics Inc Due to Vitrectomy cutters have been found not to be...
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 Synergetics Inc directly.
Affected Products
25 gauge VersaVit 2.0 Vitrectomy Cutter, Product/Part Number 70935, packaged in a Tyvek/Mylar double pouch configuration.
Quantity: 9 units
Why Was This Recalled?
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Where Was This Sold?
This product was distributed to 14 states: AL, CA, IN, KY, MI, MS, NJ, NY, OH, SC, TN, TX, UT, VA
About Synergetics Inc
Synergetics Inc has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report