Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. - Kiyohara Facility Due to Dimensions of the Luer connector parts out of...
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 Mani, Inc. - Kiyohara Facility directly.
Affected Products
MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S
Quantity: 6 units (US)
Why Was This Recalled?
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mani, Inc. - Kiyohara Facility
Mani, Inc. - Kiyohara Facility has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report