The Recall Desk
SevereFDA (Devices)·Z-2025-2020·Announced 2020-05-27

K2M Aleutian Lordotic Spreader Recalled Due to Tip Breakage Risk

K2M, Inc. is recalling Aleutian Lordotic Spreader Systems because the welded tips may break off during spinal procedures.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II and involves a structural defect (welded tip breaking off) in a medical device used during surgery, which aligns with the rubric criteria for significant injury risk or structural defects.

Plain-English summary

K2M, Inc. is recalling the Aleutian Interbody Spacer Systems, specifically the EN AN Lordotic Spreader (Catalog # 5203-90163, UDI # 10888857108769, Size 28x4mm). The recalled items are stainless steel, non-sterile instruments used to simulate cage height and expand spine disc space to determine optimal implant size based on patient anatomy.

The recall was initiated because the spreader was manufactured as two pieces welded together, a design associated with the spreader tip breaking off during the procedure. This defect poses a risk of instrument failure during surgical use.

The affected products were distributed worldwide, including nationwide in the United States (specifically Colorado, Michigan, Texas, California, New York, Florida, Maryland, Oregon, Kansas, Montana, and Missouri) and in Europe. Healthcare providers and facilities should stop using the affected Lot # FKXP units and contact the manufacturer for further instructions.

The recalled product

Product
K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90163, UDI # 10888857108769, Size 28x4mm, 12 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal impla
Manufacturer
K2M, Inc
Category
Medical Device — Surgical Instrument
Hazard

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 (1)

  • Lot # FKXP

Distribution

Distributed nationwide across the United States.

The notice also names 12 states specifically:

Part of a larger recall action

This product is one of 24 recalled by K2M, Inc 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 24 products in this recall →

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