Medical DeviceMay 20, 2026
DONJOY ICEMAN W/,UNIV,LOOP,NS,EH recall — FDA Z-2136-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Recall history in this database
Classification mix: Class II: 4.
Medical DeviceMay 20, 2026
DONJOY ICEMAN CLASSIC CUBE recall — FDA Z-2134-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Medical DeviceMay 20, 2026
DONJOY ICEMAN W/,UNIV,LOOP,NS,RH recall — FDA Z-2135-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Medical DeviceMay 20, 2026
DONJOY ICEMAN, W/COLDPAD, NS, RH recall — FDA Z-2137-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies DJO, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.