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[Recalled] K-202 GUIDE SHEATH KIT 2.0MM, model no. K-202 - Product Usage: Used with endoscopes to collect cells or tissue specimens in the respiratory organs. — Inspection confirmed a small percentage of sterile packages with inadequate pac

recall fda device japan

Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.

Recall details

ProductK-202 GUIDE SHEATH KIT 2.0MM, model no. K-202 - Product Usage: Used with endoscopes to collect cells or tissue specimens in the respiratory organs.
Brand / manufacturerAomori Olympus Co., Ltd.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1051-2021
Country of noticeJapan
Risk levelClass II
Hazard typerecall
Notice date04 January 2021

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

This Class II recall concerns device products distributed in Japan and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Aomori Olympus Co., Ltd.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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