The Recall Desk
HighFDA (Devices)·Z-1051-2021·Announced 2021-02-17

Aomori Olympus Recalls Guide Sheath Kits Due to Seal Defects

Aomori Olympus is recalling K-202 Guide Sheath Kits because some sterile packages have inadequate seals, posing an infection risk.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a risk of infection from non-sterile equipment, which is a risk-of-harm product where injury has not yet been reported, fitting the High severity criteria.

Plain-English summary

Aomori Olympus Co., Ltd. is recalling the K-202 GUIDE SHEATH KIT 2.0MM (model no. K-202). This medical device is used with endoscopes to collect cells or tissue specimens in the respiratory organs. The recall affects 260,395 units distributed nationwide in the United States, with 7,400,000 units affected globally.

The recall was initiated after inspections confirmed that a small percentage of sterile packages have inadequate package seals, specifically partial heat seals. The use of non-sterile equipment may result in patients developing infections.

Healthcare providers and facilities should stop using the affected K-202 Guide Sheath Kits and follow the instructions provided by the recalling firm for return or disposal.

The recalled product

Product
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.

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (18)

  • 01K
  • 02K
  • 03K
  • 04K
  • 05K
  • 06K
  • 07K
  • 08K
  • 09K
  • 0XK
  • 95K
  • 96K
  • 97K
  • 98K
  • 99K
  • 9XK
  • 9YK
  • 9ZK

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 111 recalled by Aomori Olympus Co., Ltd. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 111 products in this recall →