International safety notice

One of the components of the kit products we manufacture is the "Micro Feather Plastic Handle" (medical device). Feather Safety Razor Co., Ltd., which manufactures and sells this component, has confirmed that the strength of the blade fixed to the handle has increased over time. We have received reports that the blade may become weak and in some cases may fall off the handle. In addition, Feather Safety Razor Co., Ltd. has announced that similar defects may occur in products manufactured after May 2022. As we have received a report that we are implementing a voluntary recall of the affected products because we cannot deny the We have decided to voluntarily recall the product.

Japan / PMDA Recalls · JPN · Aug 29, 2023

Key facts

Title One of the components of the kit products we manufacture is the "Micro Feather Plastic Handle" (medical device). Feather Safety Razor Co., Ltd., which manufactures and sells this component, has confirmed that the strength of the blade fixed to the handle has increased over time. We have received reports that the blade may become weak and in some cases may fall off the handle. In addition, Feather Safety Razor Co., Ltd. has announced that similar defects may occur in products manufactured after May 2022. As we have received a report that we are implementing a voluntary recall of the affected products because we cannot deny the We have decided to voluntarily recall the product.
Regulator Japan / PMDA Recalls
Country JPN
Brand Common Name: Single Use Class III Treatment Kit Sales name: Ophthalmology kit N
Manufacturer Livedo Corporation Co., Ltd.
Models 221108101, 230424101, 230707101, 230307101, 230606101, 230324101, 221101101, 221125201, 220912201, 230419101, 221207101, 120213100307 and 17 more
Date Aug 29, 2023
Regulator page info.pmda.go.jp

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About International device safety notices

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Source: National medical device regulators (as listed), compiled by Orca1

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