# FDA recall Z-2134-2026

> **DJO, LLC** · Class II · device recall initiated 2026-03-19.

## Product

Brand Name: DONJOY  Product Name: ICEMAN CLASSIC CUBE  Model/Catalog Number: 11-0494  Software Version: no  Product Description: 11-0494 - ICEMAN CLASSIC CUBE  The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan¿ helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology.  Component: no

## Reason for recall

Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

## Distribution

Worldwide - U.S. Nationwide distribution in the states of AK, AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MO, NC, NE. NY, OH, OK, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WV. The country of Canada.

## Key facts

- **Recall number:** Z-2134-2026
- **Recalling firm:** DJO, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-19
- **Report date:** 2026-05-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Carlsbad, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2134-2026

## Citation

> MORVS. FDA recall Z-2134-2026. Retrieved 2026-10-15 from https://api.morvs.ai/recall/Z-2134-2026. Source: US FDA. Licensed CC0.

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