Mani, Inc. - Kiyohara Facility recalls MANI TROCAR KIT 23G S - Product Usage: for use in injecting
Recalled Product
MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S
Hazard / Issue
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot Codes: V180077300, Exp Date: 2020/10 and V200009500, EXp Date: 2022/03
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