FDA recall: Brand Name: DONJOY

The FDA has classified an open recall of the DJO DONJOY ICEMAN CLASSIC CUBE cold therapy unit (Model 11-0494) due to a defective connector that can interrupt the delivery of cold therapy. This device is commonly used in rehabilitation settings to manage pain and swelling following injury or surgery. Clinicians using this unit should review the recall notice and follow DJO's guidance regarding affected devices.

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