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Mani, Inc. - Kiyohara Facility recalls MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during oph
Recalled December 16, 2020 · FDA recall Z-0557-2021 · Mani, Inc. - Kiyohara Facility
Hazard
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use · FDA Class II
Units
6 units (US)
Sold at
US Nationwide distribution in the state of MO.
Description
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
Product
MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S
Manufacturer(s)
Mani, Inc. - Kiyohara Facility
Made in
Japan
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →