DJO recalls
5 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for DJO and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-05-20FDA-DeviceClass IIDJO IceMan cold therapy unit recalled for connector failure
Some DJO IceMan CLASSIC3 cold therapy units (model 11-9099, lot 110525) have a broken connector that may temporarily interrupt cold therapy during treatment. No injuries have been reported. The issue affects about 96 units distributed across the US and Canada.
- 2026-05-20FDA-DeviceClass IIDJO DONJOY IceMan CLASSIC3 recalled for broken connector
Some DJO DONJOY IceMan CLASSIC3 cold therapy units (model 11-1424) have a broken connector that can interrupt cold therapy temporarily. This affects prescribed rehabilitation treatments. No injuries have been reported.
- 2026-05-20FDA-DeviceClass IIDJO DONJOY ICEMAN cold therapy unit recalled for connector failure
Some DJO DONJOY ICEMAN CLASSIC3 cold therapy units (model 11-1422) may have a broken connector that could temporarily stop the cold therapy from working as prescribed. The connector failure affects specific production lots and has been identified in devices distributed across the U.S. and Canada. No injuries have been reported.
- 2026-05-20FDA-DeviceClass IIDJO DONJOY ICEMAN CLASSIC CUBE recalled for connector failure
Some DONJOY ICEMAN CLASSIC CUBE cold therapy units (model 11-0494) contain a broken connector that may temporarily interrupt cold therapy during treatment. This affects units from specific lot codes distributed across the U.S. and Canada. No injuries have been reported.
- 2025-12-03FDA-DeviceClass IICold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures capable of causing a second degree burn.
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