Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals on the outer pouch of various,...
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
25ga Endo Illuminator, Synergetics, inc., length 7.0 ft, sterile / EO, 56.02.25 Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Quantity: 96 units
Why Was This Recalled?
Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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