WhichRecall
Class IIReported 2025-12-03

Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02

Recalled by DJO, LLC

Reason for Recall

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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Recall Number
Z-0722-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-09-25
Reported
2025-12-03
Distribution
US Nationwide distribution in the states of WI, TN, TX, MD, GA, UT, WA, MI, NC, NE, CA, MA, CO, SC, OH, IN, MN, NM, PA, NY, IL, FL, NJ, VA, AZ, VT, CT, OK.
Code Info
REF/UDI-DI/Lot: DP163CT02/00888912164382/190523, 171221. DP163CT03-BLK-L,XL/00888912164481/150221, 180821
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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