Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2134-2026 — 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 t

U.S. FDA — Device Enforcement · United States · 2026-03-19 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2134-2026
Date of alert: 2026-03-19
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: DJO, LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00888912003100

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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