Regulator FDA — DJO, LLC device-recallcold-therapyrehabilitation
FDA recall: Brand Name: DONJOY
The FDA has classified an open recall of the DonJoy IceMan CLASSIC3 cold therapy unit (model 11-1422) due to a defective connector that can interrupt the delivery of cold therapy. The device is used in rehabilitation settings to help manage pain and swelling following injury or surgery. Physical therapists who utilize this device in their practice should check whether affected units are in use.
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