Mani, Inc. - Kiyohara Facility: Medical Device Recalls in 2020
Updated on March 25, 2026.
According to to data from the FDA, there were 2 medical device recalls made by Mani, Inc. - Kiyohara Facility in 2020. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S
- MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery Ref: MTC 23S