DONJOY PERFORMANCERecalls & reported problems across all models

We found 2 models of DONJOY PERFORMANCE by Djo, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

DONJOY PERFORMANCE recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Sep 25, 2025Class IIOpen, Classified

   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.

   Z-0722-2026 · Root cause: Labeling Change Control · names 2 of these models · Recall details · FDA record ↗

DONJOY PERFORMANCE models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• DONJOY PERFORMANCE DP163CT02

  Pack, hot or cold, reusable
  1 recall0 reports
• DONJOY PERFORMANCE DP163CT03-BLK-L,XL

  Pack, hot or cold, reusable
  1 recall0 reports

Other Djo, LLC products

• DONJOY11 models · 10 reports · 4 recalls
• CHATTANOOGA39 models · 122 reports
• DJO SURGICAL42 models · 98 reports
• AIRCAST7 models · 10 reports · 1 recall