Agency classClass IIOur severity:High FDA (Devices)·Z-0993-2021·Announced 2021-02-17

Aomori Olympus ForceMax Injector Recalled for Inadequate Package Seals

Aomori Olympus is recalling ForceMax injectors because inspection found some sterile packages had inadequate seals, posing an infection risk if non-sterile equipment is 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 the source text does not report specific injuries or illnesses, aligning with the 'High' severity criteria for risk-of-harm products without reported injury.

Plain-English summary

Aomori Olympus Co., Ltd. is recalling the INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM (model no. NM-400L-0421). 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 was initiated after inspection confirmed that a small percentage of sterile packages had inadequate package seals, specifically partial heat seals. The source text notes that patients may develop infections if non-sterile equipment is used.

The recall involves 260,395 units in the United States, with a total of 7,400,000 units affected globally. The affected units were distributed nationwide in the US. Affected lot codes include 01K, 02K, 03K, 04K, 05K, 07K, 08K, 09K, 98K, 99K, 9XK, 9YK, ZK, 05V, 06V, 07V, 08V, 09V, and 0XV. Healthcare providers should stop using the affected devices and contact the manufacturer for instructions on return or replacement.

The recalled product

Product: INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM, model no. NM-400L-0421 - 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 Injection Device
Hazard: infection
sterility-failure

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 →

Same manufacturer · Aomori Olympus Co., Ltd.

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Same hazard · infection