Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0722-2026 — Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02

U.S. FDA — Device Enforcement · United States · 2025-09-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0722-2026
Date of alert
2025-09-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
DJO, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00888912164382
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.