Mani, Inc. - Kiyohara Facility: Medical Device Recall in 2020 - (Recall #: Z-0557-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S

Product Classification:

Class II

Date Initiated: October 27, 2020

Date Posted: December 16, 2020

Recall Number: Z-0557-2021

Event ID: 86873

Reason for Recall:

Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use

Status: Terminated

Product Quantity: 6 units (US)

Code Information:

Lot Codes: V180077300, Exp Date: 2020/10 and V200009500, EXp Date: 2022/03

Distribution Pattern:

US Nationwide distribution in the state of MO.

Voluntary or Mandated:

Voluntary: Firm initiated