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Mani, Inc. - Kiyohara Facility Recalls
3 recalls on record · December 16, 2020 to May 3, 2023 · Medical Devices
Recalls by year
20
23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 3, 2023Medical DevicesFDA
Mani, Inc. - Kiyohara Facility recalls Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3
Hazard: A packaging defect may compromise the sterile barrier.
December 16, 2020Medical DevicesFDA
Mani, Inc. - Kiyohara Facility recalls MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials duri
Hazard: Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
December 16, 2020Medical DevicesFDA
Mani, Inc. - Kiyohara Facility recalls MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during oph
Hazard: Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use