Agency classClass IIOur severity:High FDA (Devices)·Z-1025-2021·Announced 2021-02-17

Aomori Olympus Endoscopic Injector Recall Due to Package Seal Defects

Aomori Olympus is recalling specific endoscopic injectors because inspection found some sterile packages had inadequate seals, posing a risk of infection if used.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

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-harm product (infection from non-sterile equipment) where no specific injuries or illnesses have been reported yet, fitting the 'High' severity criteria for theoretical risk without confirmed harm.

Plain-English summary

Aomori Olympus Co., Ltd. is recalling the INJECTOR FORCEMAX UP 2MM CH 25G 4MM (model no. NM-401L-0425). This medical device is used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. The recall covers 260,395 units distributed in the United States, with a global total of 7,400,000 units. The affected units are identified by specific lot codes including 01K through 08K, 98K through 9ZK, and 05V through 0XV.

The recall was initiated after inspection confirmed that a small percentage of sterile packages had inadequate package seals, specifically partial heat seals. The use of non-sterile equipment in these procedures may lead to patient infections.

Healthcare providers and facilities should stop using the affected injectors immediately. Users should check their inventory for the specific model number and lot codes listed in the recall notice to identify affected units.

The recalled product

Product: INJECTOR FORCEMAX UP 2MM CH 25G 4MM, model no. NM-401L-0425 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
Manufacturer: Aomori Olympus Co., Ltd.
Category: Medical Device — Endoscopic Instrument
Hazard: infection
packaging-defect

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 (19)

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 →

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Same hazard · infection