The Recall Desk
ModerateFDA (Devices)·Z-2136-2026·Announced 2026-05-20

DonJoy IceMan CLASSIC3 Cold Therapy Unit Connector Fault Recall

DJO, LLC is recalling the DonJoy IceMan CLASSIC3 cold therapy unit (Model 11-1424) due to a broken connector that may interrupt prescribed cold therapy treatment.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: This is an FDA Class II recall of a medical device with no reported illnesses or injuries. The hazard—a temporary interruption of therapy—is a functional defect without documented harm, placing it in the Moderate category per the rubric.

Plain-English summary

DJO, LLC is recalling the DonJoy IceMan CLASSIC3 cold therapy unit, Model 11-1424, distributed nationwide in the United States and Canada. The device is used to reduce pain and swelling and aid rehabilitation through cold therapy administered as directed by a medical professional.

The recall is due to a broken connector in the device that may result in a temporary interruption of prescribed cold therapy. Approximately 480 units with Lot Code 110525 are affected by this issue.

Consumers should contact DJO, LLC regarding their affected unit. The recalling firm can provide guidance on obtaining a replacement or repair.

The recalled product

Product
Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product Description: 11-1424 - ICEMAN W/,UNIV,LOOP,NS,EH The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMa
Manufacturer
DJO, LLC
Category
Medical Device — Cold Therapy Equipment
Hazard
Affected units
480

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)

  • Model/Catalog Number: 11-1424 Lot Code: Lot: 110525 GTIN: 00888912017305

Distribution

Distributed nationwide across the United States.

The notice also names 32 states specifically:

Part of a larger recall action

This product is one of 4 recalled by DJO, LLC 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 4 products in this recall →

Related recalls

Same manufacturer · DJO, LLC

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Same hazard · connector failure

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